630-580-1088 sales@ambeed.com
Structure Search

List Search MOL Search Structure Search

0
Chemistry
Boronic acids/esters >>1,3,2-DioxaborinaneAliphatic BoronsAromatic BoronsBCATBoric AcidsMIDA BoronatesOther BoronatesOther BoronsOxaborolesCatalysis Chemistry >>Achiral Crown LigandsC-H ActivationCarbon-Donor LigandsChiral Carbon LigandsChiral Crown LigandsChiral Olefin LigandsCross-CouplingCross-Coupling Using Transition Metal CatalystsDACH or Trost LigandsChemical Biology >>Conjugation Chemistry
GlycoscienceLinkers and CrosslinkersNucleic Acid ChemistryPEGylationPeptide ChemistryPhotolabile Protecting GroupHeterocyclic Building Blocks >>AcridinesAliphatic HeterocyclesAromatic HeterocyclesAzetidinesBenzimidazolesBenzisoxazolesBenzodioxansBenzofuransBenzothiazolesInorganic reagents >>Inorganic ReagentOrganic Building Blocks >>Acid AnhydridesAcyl ChloridesAlcohols
AldehydesAliphatic Chain HydrocarbonsAliphatic Cyclic HydrocarbonsAlkenesAlkylsAlkynesOrganometallic Reagents >>Grignard ReagentsOrganoarsenicOrganobismuthOrganoboronOrganogermaniumOrganolithiumOrganomercuryOrganosiliconOrganotinSpecialty Synthesis >>Enzyme-Mediated SynthesisFluorous SynthesisIonic LiquidsSolid Supported SynthesisStains and Dyes >>
Acid DyesAzoic DyesBasic DyesDirect DyesDisperse DyesDye IntermediatesMordant DyesOil DyesOther Stains and DyesSynthetic Reagents >>Acids and BasesC-C Bond FormationC-X Bond Formation (Halogen)C-X Bond Formation (Non-Halogen)Chelation and Complexation CompoundsCondensation AgentsCouplingDehydrating ReagentsFluorination Reagent
Pharmaceutical Intermediates
Analgesics >>BenzhydrocodoneBicifadineCapsaicinCelecoxibDebio-0827DexamethasoneElagolix SodiumEsketamine HydrochlorideIbuprofen SodiumAnesthetics >>CiprofolEsketamine HydrochlorideFospropofol Fospropofol DisodiumLevobupivacaine RemimazolamRemimazolam BesilateRemimazolam BesylateRopivacaineAnti-Addiction Agents >>Kakonein
Lofexidine HydrochlorideVarenicline Anti-inflammatory Agents >>ApremilastAsunaprevirATB-346 RelatedBalsalazide BaricitinibBencycloquidium BromideBudesonideCefiderocol Sulfate TosylateCeftaroline Fosamil AcetateAntibacterials >>AFN-1252 RelatedAlatrofloxacin Bedaquiline FumarateBesifloxacin BrilacidinCaspofungin AcetateCefiderocol Sulfate TosylateCefilavancinCeftaroline Fosamil
Anticonvulsants >>BrivaracetamCannabidiolEscitalopram OxalateEslicarbazepine Acetate RelatedFosphenytoinGabapentin EnacarbilJNJ-10234094LacosamideLevetiracetam RelatedAntidementia Agents >>Azeliragon RelatedDavunetideDonepezil HydrochlorideDonepezil RelatedEnsaculinFlorbetaben Flortaucipir F 18Flutemetamol IdalopirdineAntidepressants >>4-Chlorokynurenine
AgomelatineAgomelatine RelatedAllopregnanolone RelatedAmibegronAmitifadineAripiprazole RelatedBasimglurantBefloxatoneAntiemetics >>AprepitantAprepitant RelatedDolasetron RelatedDolasetron Mesylate HydrateFosaprepitant DimeglumineFosaprepitant RelatedOlanzapinePalonosetron RelatedPalonosetron HydrochlorideAntifungals >>Anidulafungin RelatedCabotegravirMore >>
Inhibitors/Agonists
ADC >>ADC AntibodyADC LinkerADC Linker with PayloadADC ToxinAntibody-Drug Conjugates (ADCs)Drug-Linker Conjugates for ADCAngiogenesis >>ALKBcr-AblBTKEGFRFAKFGFRFLT3HER2HIFAnti-infection >>3CLproAntibacterialAntibioticAntifungal
AntiparasiticAntiprotozoalAntiviralArenavirusBVDVApoptosis >>Apoptosis InducerBcl-2Bcl-6BRKc-Mycc-RETC/EBPCARDCaspaseAutophagy >>Atg4ATG4BATTECsAUTACsAutophagyBeclin1
FKBPLC3LRRK2Biochemical Reagent >>Cell Cycle >>AntifolateAPCAurora KinaseBUBCasein KinaseCdc25CDKChkCRISPR/Cas9Cytoskeleton >>ActinArp2/3 ComplexCYTHCytoplasmic DyneinDynaminFAKMore >>
Material Science
Aggregation-Induced Emission >>Other AIE BlocksTetraphenylethylene SeriesCOFs Linkers >>Aldehyde COFs LinkersAlkynyl COFs LinkersAmine COFs LinkersBoric COFs LinkersCyano COFs LinkersMultifunctional COFs linkersOther COFs linkersTriptycene SeriesElectronic Materials >>Battery MaterialsDye-Sensitized Solar Cell (DSSC) MaterialsElectronic MaterialLiquid Crystal (LC) MaterialsMolecular ConductorsOrganic Light-Emitting Diode (OLED) MaterialsOrganic Solar Cell (OPV) MaterialsOrganic Transistor (OFET) MaterialsPerovskite Solar Cell (PSC) MaterialsMagnetic Materials >>Magnetic Ionic LiquidsMagnetic MaterialMagnetic Metal Complexes
Organic Radicals Material Chemical Compounds >>Ligands for Functional Metal ComplexesLiquid Crystal (LC) Building BlocksPhthalocyanine Building BlocksPolymer and Macromolecule Semiconductor Building BlocksSmall Molecule Semiconductor Building BlocksSolubility Enhancing Reagents Supramolecular Host Materials MOF Ligands >>Carboxylic Acid MOF LigandsCarboxylic Acid Nitrogen-Containing Mixed MOF LigandsNitrogen-Containing MOF LigandsOther MOF LigandsNanomaterials >>Carbon NanomaterialsCeramic MembranesDendrimersGold NanoparticlesIron Oxide NanoparticlesMaterials by ApplicationMesoporous MaterialsMetals and Metal AlloysNano Minerals: NanoclaysOLED Materials >>Dopant
HostHTMOLED IntermediatesOther OLED related materialsOptical Materials >>Coumarin DyesCyanine and Squarylium DyesDCM DyesDipyrromethene DyesFluorescence MaterialsFluorescent ProbesHeat and Pressure Sensitive DyesNear-Infrared (NIR) DyesOrganic Non-Linear Optical (NLO) MaterialsOrganic Pigments >>Organic PigmentOther Materials >>Material OtherPolymer Science >>MonomersPolymer AdditivesPolymerization ReagentsPolymersResins
Contact Us
Home Cart 0 Sign in  
X
Chemistry
Organic Building Blocks
Aryls
3-iodophenol
3-Chloro-5-iodophenol
Chemistry
Organic Building Blocks
Aryls
Chlorides Fluorinated Building Blocks Phenols Iodides Benzene Compounds
3-iodophenol
fluorobenzene Chlorobenzene 3-chlorophenol iodophenol benzyl 1-chloro-3-iodobenzene

[ CAS No. 861347-86-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
3d Animation Molecule Structure of 861347-86-6
Chemical Structure| 861347-86-6
Chemical Structure| 861347-86-6
Structure of 861347-86-6 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

For Research Only 120K+ Compounds Competitive Price 1-2 Day Shipping

Quality Control of [ 861347-86-6 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 861347-86-6 ]

SDS Specification
Alternatived Products of [ 861347-86-6 ]
Product Citations

Product Details of [ 861347-86-6 ]

CAS No. :861347-86-6 MDL No. :MFCD12405417
Formula : C6H4ClIO Boiling Point : -
Linear Structure Formula :- InChI Key :QBNIBNUEBBJVFN-UHFFFAOYSA-N
M.W : 254.45 Pubchem ID :53425564
Synonyms :

Safety of [ 861347-86-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 861347-86-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 861347-86-6 ]

[ 861347-86-6 ] Synthesis Path-Downstream   1~1

  • 1
  • 3-chloro-5-iodophenol [ No CAS ]
  • [ 1338225-97-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 5 steps 1.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 20 - 60 °C 2.1: potassium hydroxide / <i>tert</i>-butyl alcohol / 1 h / 75 °C 2.2: 0 °C / pH 5 3.1: N,N-dimethyl-formamide / 17 h / 120 °C / Inert atmosphere 4.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C 5.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 0 - 20 °C
Multi-step reaction with 5 steps 1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 12 h / 45 - 55 °C / Large scale 2: sodium hydroxide / <i>tert</i>-butyl alcohol / 38 h / 65 - 75 °C / Large scale 3: copper(l) cyanide / 1-methyl-pyrrolidin-2-one / 40 h / 105 - 110 °C / Large scale 4: potassium carbonate / N,N-dimethyl-formamide / 9 h / -10 - 10 °C / Large scale 5: potassium carbonate / water; 1-methyl-pyrrolidin-2-one / 34 h / 5 - 10 °C / Inert atmosphere; Large scale
Reference： [1]Current Patent Assignee: MERCK & CO INC - US2011/245296, 2011, A1
[2]Campeau, Louis-Charles; Chen, Qinghao; Gauvreau, Danny; Girardin, Mélina; Belyk, Kevin; Maligres, Peter; Zhou, Guoyue; Gu, Chaozhan; Zhang, Wei; Tan, Lushi; O'Shea, Paul D. [Organic Process Research and Development, 2016, vol. 20, # 8, p. 1476 - 1481]

Tags: 861347-86-6 synthesis path| 861347-86-6 SDS| 861347-86-6 COA| 861347-86-6 purity| 861347-86-6 application| 861347-86-6 NMR| 861347-86-6 COA| 861347-86-6 structure

Recommend Products
Same Skeleton Products
Related Products
Isomers
Categories
Chemistry
Organic Building Blocks
Benzene Compounds
Chlorobenzene
Chemistry
Organic Building Blocks
Benzene Compounds
benzyl
Chemistry
Organic Building Blocks
Chlorides
1-chloro-3-iodobenzene
Chemistry
Organic Building Blocks
Chlorides
3-chlorophenol
Chemistry
Organic Building Blocks
Fluorinated Building Blocks
fluorobenzene
Chemistry
Organic Building Blocks
Iodides
1-chloro-3-iodobenzene
Chemistry
Organic Building Blocks
Iodides
3-iodophenol
Chemistry
Organic Building Blocks
Iodides
iodophenol
Chemistry
Organic Building Blocks
Phenols
3-chlorophenol
Chemistry
Organic Building Blocks
Phenols
3-iodophenol
Chemistry
Organic Building Blocks
Phenols
iodophenol
Chemistry
Organic Building Blocks
Aryls

Technical Information

• Acid-Catalyzed α -Halogenation of Ketones • Acidity of Phenols • Addition of a Hydrogen Halide to an Internal Alkyne • Alcohols from Haloalkanes by Acetate Substitution-Hydrolysis • Alcohols React with PX3 • Alkyl Halide Occurrence • Alkylation of an Alkynyl Anion • An Alkane are Prepared from an Haloalkane • Benzylic Oxidation • Birch Reduction • Birch Reduction of Benzene • Blanc Chloromethylation • Chan-Lam Coupling Reaction • Chloroalkane Synthesis with SOCI2 • Complete Benzylic Oxidations of Alkyl Chains • Complete Benzylic Oxidations of Alkyl Chains • Conjugate Additions of p-Benzoquinones • Conversion of Amino with Nitro • Convert Haloalkanes into Alcohols by SN2 • Decomposition of Arenediazonium Salts to Give Phenols • Deprotonation of Methylbenzene • Diazo Coupling • Directing Electron-Donating Effects of Alkyl • Electrophilic Chloromethylation of Polystyrene • Electrophilic Substitution of the Phenol Aromatic Ring • Etherification Reaction of Phenolic Hydroxyl Group • Friedel-Crafts Alkylation of Benzene with Acyl Chlorides • Friedel-Crafts Alkylation of Benzene with Carboxylic Anhydrides • Friedel-Crafts Alkylation of Benzene with Haloalkanes • Friedel-Crafts Alkylation Using Alkenes • Friedel-Crafts Alkylations of Benzene Using Alkenes • Friedel-Crafts Alkylations Using Alcohols • Friedel-Crafts Reaction • General Reactivity • Grignard Reaction • Groups that Withdraw Electrons Inductively Are Deactivating and Meta Directing • Halogenation of Alkenes • Halogenation of Benzene • Halogenation of Phenols • Hiyama Cross-Coupling Reaction • Hydrogenation to Cyclohexane • Hydrogenolysis of Benzyl Ether • Kinetics of Alkyl Halides • Kolbe-Schmitt Reaction • Kumada Cross-Coupling Reaction • Methylation of Ammonia • Nitration of Benzene • Nucleophilic Aromatic Substitution • Nucleophilic Aromatic Substitution with Amine • Oxidation of Alkyl-substituted Benzenes Gives Aromatic Ketones • Oxidation of Phenols • Pechmann Coumarin Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Dihalides • Reductive Removal of a Diazonium Group • Reimer-Tiemann Reaction • Reverse Sulfonation——Hydrolysis • Stille Coupling • Substitution and Elimination Reactions of Alkyl Halides • Sulfonation of Benzene • Suzuki Coupling • The Acylium Ion Attack Benzene to Form Phenyl Ketones • The Claisen Rearrangement • The Nitro Group Conver to the Amino Function • Vilsmeier-Haack Reaction
Historical Records

Related Functional Groups of
[ 861347-86-6 ]

Aryls

Chemical Structure| 861800-86-4

[ 861800-86-4 ]

1-Chloro-3-iodo-5-methoxybenzene

Similarity: 0.88

Chemical Structure| 1807182-53-1

[ 1807182-53-1 ]

3,4-Dichloro-5-iodophenol

Similarity: 0.85

Chemical Structure| 1805483-32-2

[ 1805483-32-2 ]

2,3-Dichloro-5-iodophenol

Similarity: 0.85

Chemical Structure| 855403-42-8

[ 855403-42-8 ]

3-Chloro-4-iodophenol

Similarity: 0.84

Chemical Structure| 136808-72-5

[ 136808-72-5 ]

5-Chloro-2-iodophenol

Similarity: 0.84

Chlorides

Chemical Structure| 861800-86-4

[ 861800-86-4 ]

1-Chloro-3-iodo-5-methoxybenzene

Similarity: 0.88

Chemical Structure| 1807182-53-1

[ 1807182-53-1 ]

3,4-Dichloro-5-iodophenol

Similarity: 0.85

Chemical Structure| 1805483-32-2

[ 1805483-32-2 ]

2,3-Dichloro-5-iodophenol

Similarity: 0.85

Chemical Structure| 855403-42-8

[ 855403-42-8 ]

3-Chloro-4-iodophenol

Similarity: 0.84

Chemical Structure| 136808-72-5

[ 136808-72-5 ]

5-Chloro-2-iodophenol

Similarity: 0.84

Iodides

Chemical Structure| 861800-86-4

[ 861800-86-4 ]

1-Chloro-3-iodo-5-methoxybenzene

Similarity: 0.88

Chemical Structure| 1807182-53-1

[ 1807182-53-1 ]

3,4-Dichloro-5-iodophenol

Similarity: 0.85

Chemical Structure| 1805483-32-2

[ 1805483-32-2 ]

2,3-Dichloro-5-iodophenol

Similarity: 0.85

Chemical Structure| 855403-42-8

[ 855403-42-8 ]

3-Chloro-4-iodophenol

Similarity: 0.84

Chemical Structure| 136808-72-5

[ 136808-72-5 ]

5-Chloro-2-iodophenol

Similarity: 0.84

; ;