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[ CAS No. 1807164-93-7 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
3d Animation Molecule Structure of 1807164-93-7
Chemical Structure| 1807164-93-7
Chemical Structure| 1807164-93-7
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Quality Control of [ 1807164-93-7 ]

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Product Citations

Product Details of [ 1807164-93-7 ]

CAS No. :1807164-93-7 MDL No. :MFCD28736490
Formula : C7H5BrN2O Boiling Point : -
Linear Structure Formula :- InChI Key :BMSFODZYNGNTIA-UHFFFAOYSA-N
M.W : 213.03 Pubchem ID :118850787
Synonyms :

Calculated chemistry of [ 1807164-93-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.14
TPSA : 45.91 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.25 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.79
Log Po/w (XLOGP3) : 1.9
Log Po/w (WLOGP) : 1.72
Log Po/w (MLOGP) : 0.68
Log Po/w (SILICOS-IT) : 1.98
Consensus Log Po/w : 1.62

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.7
Solubility : 0.43 mg/ml ; 0.00202 mol/l
Class : Soluble
Log S (Ali) : -2.49
Solubility : 0.694 mg/ml ; 0.00326 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.1
Solubility : 0.17 mg/ml ; 0.000798 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.09

Safety of [ 1807164-93-7 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501 UN#:3439
Hazard Statements:H301-H311-H331 Packing Group:
GHS Pictogram:
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Technical Information

• Acetal Formation • Acid-Catalyzed α -Halogenation of Ketones • Add Hydrogen Cyanide to Aldehydes and Ketones to Produce Alcohols • 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 • Amine Synthesis from Nitriles • Amine Synthesis from Nitriles • An Alkane are Prepared from an Haloalkane • Blaise Reaction • Catalytic Hydrogenation • Chichibabin Reaction • Complex Metal Hydride Reductions • Convert Haloalkanes into Alcohols by SN2 • Cyanohydrins can be Convert to Carbonyl Compounds under Basic Conditions • DIBAL Attack Nitriles to Give Ketones • Esters Are Reduced by LiAlH4 to Give Alcohols • Esters Hydrolyze to Carboxylic Acids and Alcohols • Ether Synthesis by Oxymercuration-Demercuration • Ethers Synthesis from Alcohols with Strong Acids • Friedel-Crafts Alkylation of Benzene with Haloalkanes • General Reactivity • Grignard Reaction • Grignard Reagents Transform Esters into Alcohols • Halogenation of Alkenes • Hantzsch Pyridine Synthesis • Hiyama Cross-Coupling Reaction • Hydride Reductions • Ketone Synthesis from Nitriles • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Methylation of Ammonia • Methylation of Ammonia • Nitriles Hydrolyze to Carboxylic Acids • Nomenclature of Ethers • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Ethers • Primary Ether Cleavage with Strong Nucleophilic Acids • Pyridines React with Grignard or Organolithium Reagents • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Dihalides • Reactions of Ethers • Ring Opening of Oxacyclopropane • Ritter Reaction • Stille Coupling • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Synthesis of Alcohols from Tertiary Ethers • The Cycloaddition of Dienes to Alkenes Gives Cyclohexenes • The Nucleophilic Opening of Oxacyclopropanes • Thorpe-Ziegler Reaction • Williamson Ether Syntheses
Historical Records

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[ 1807164-93-7 ]

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