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Chemistry
Organic Building Blocks
Chlorides
chloromethyl
1-(Chloromethyl)-4-(octyloxy)benzene
Chemistry
Organic Building Blocks
Chlorides
Benzyl Chlorides Benzene Compounds
chloromethyl
benzyl

[ CAS No. 110482-75-2 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
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3d Animation Molecule Structure of 110482-75-2
Chemical Structure| 110482-75-2
Chemical Structure| 110482-75-2
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Quality Control of [ 110482-75-2 ]

COA NMR CNMR HPLC LC-MS

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SDS Specification
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Product Citations

Product Details of [ 110482-75-2 ]

CAS No. :110482-75-2 MDL No. :MFCD11197432
Formula : C15H23ClO Boiling Point : -
Linear Structure Formula :- InChI Key :OFVQMKNVOIJMNJ-UHFFFAOYSA-N
M.W : 254.80 Pubchem ID :14674286
Synonyms :

Safety of [ 110482-75-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501 UN#:3265
Hazard Statements:H302-H314 Packing Group:Ⅱ
GHS Pictogram:

Application In Synthesis of [ 110482-75-2 ]

* 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 [ 110482-75-2 ]

[ 110482-75-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 99-24-1 ]
  • [ 110482-75-2 ]
  • C53H74O8 [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 17h;
Reference： [1]Percec, Virgil; Won, Betty C.; Peterca, Mihai; Heiney, Paul A. [Journal of the American Chemical Society, 2007, vol. 129, # 36, p. 11265 - 11278]
  • 2
  • [ 2150-43-8 ]
  • [ 110482-75-2 ]
  • [4-3,4]8G1COOCH3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With potassium carbonate In N,N-dimethyl-formamide 26 Example 26; Preparation of [4-3,4]8G1COOCH3 Dendrimer Example 26 Preparation of [4-3,4]8G1COOCH3 Dendrimer This compound was synthesised following the same general procedure as that for the preparation of [4-3,4]MeG1CO2CH3; K2CO3 (15.7 g, 114 mmol), methyl 3,4-dihydroxybenzoate (4.29 g, 25.5 mmol), 4-octyloxybenzyl chloride (13.0 g, 51 mmol), DMF (120 mL). TLC (CH2Cl2), flash column chromatography: silica gel/CH2Cl2, yield: 12.4 g (80%) of the title compound as a white solid. mp 42-44° C. 1H NMR (300 MHz, CDCl3) δ=7.63 (m, 2H), 7.33 (t, 4H, J=8.7 Hz), 6.92 (d, 1H, J=8.1 Hz), 6.87 (d, 4H, J=6.9 Hz), 5.09 (d, 4H, J=6.6 Hz), 3.94 (t, 4H, J=6.6 Hz), 3.86 (s, 3H), 1.79-1.72 (m, 4H), 1.43 (m, 4H), 1.38-1.27 (m, 16H), 0.87 (t, 6H, J=6.5 Hz). 13C NMR (75 MHz, CDCl3) δ=167.0, 159.2, 153.2, 148.6, 129.3, 129.1, 128.9, 128.5, 124.1, 123.1, 115.9, 114.7 (*2), 113.6, 71.3, 70.9, 68.2, 52.1, 32.0, 29.6, 29.5, 29.4, 26.2, 22.8, 14.3.
Reference： [1]Current Patent Assignee: UNIVERSITY OF PENNSYLVANIA - US2006/88499, 2006, A1 Location in patent: Page/Page column 48

Tags: 110482-75-2 synthesis path| 110482-75-2 SDS| 110482-75-2 COA| 110482-75-2 purity| 110482-75-2 application| 110482-75-2 NMR| 110482-75-2 COA| 110482-75-2 structure

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Chemistry
Organic Building Blocks
Benzene Compounds
benzyl
Chemistry
Organic Building Blocks
Chlorides
chloromethyl
Chemistry
Organic Building Blocks
Benzyl Chlorides

Technical Information

• Acid-Catalyzed α -Halogenation of Ketones • Addition of a Hydrogen Halide to an Internal Alkyne • Alcohols from Haloalkanes by Acetate Substitution-Hydrolysis • Alkyl Halide Occurrence • Alkylation of an Alkynyl Anion • An Alkane are Prepared from an Haloalkane • Benzylic Halogenation • Benzylic Oxidation • Birch Reduction • Birch Reduction of Benzene • Blanc Chloromethylation • Chloroalkane Synthesis with SOCI2 • Complete Benzylic Oxidations of Alkyl Chains • Complete Benzylic Oxidations of Alkyl Chains • Conversion of Amino with Nitro • Convert Haloalkanes into Alcohols by SN2 • Deprotonation of Methylbenzene • Directing Electron-Donating Effects of Alkyl • Electrophilic Chloromethylation of Polystyrene • 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 • Hiyama Cross-Coupling Reaction • Hydrogenation to Cyclohexane • Hydrogenolysis of Benzyl Ether • Kinetics of Alkyl Halides • 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 • Preparation of Alkylbenzene • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reductive Removal of a Diazonium Group • 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
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