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6-Bromo-2,3-difluorobenzenemethanol is a chemical compound that features a benzene ring with two fluorine atoms and a bromine atom attached, along with a hydroxyl group. This unique structure endows it with potential applications in various fields.
Used in Pharmaceutical Industry:
6-Bromo-2,3-difluorobenzenemethanol is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structural properties make it valuable for the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
6-BROMO-2,3-DIFLUOROBENZENEMETHANOL also serves as an intermediate in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products to improve crop protection and yield.
Used in Medicinal Chemistry:
6-Bromo-2,3-difluorobenzenemethanol is utilized in medicinal chemistry for its potential role in drug discovery. Its distinct structural features allow for the exploration of new therapeutic agents and treatments.
Used in Material Science:
6-BROMO-2,3-DIFLUOROBENZENEMETHANOL has potential applications in the development of new materials, where its unique properties can be leveraged to create innovative products with specialized functions.
Used in Chemical Process Development:
6-Bromo-2,3-difluorobenzenemethanol may also be employed in the development of new chemical processes, where its reactive sites can be harnessed to improve synthesis methods and reaction efficiencies.

651326-72-6

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651326-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651326-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,3,2 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 651326-72:
(8*6)+(7*5)+(6*1)+(5*3)+(4*2)+(3*6)+(2*7)+(1*2)=146
146 % 10 = 6
So 651326-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrF2O/c8-5-1-2-6(9)7(10)4(5)3-11/h1-2,11H,3H2

651326-72-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-bromo-2,3-difluorophenyl)methanol

1.2 Other means of identification

Product number -
Other names 6-Bromo-2,3-difluorobenzenemethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:651326-72-6 SDS

651326-72-6Relevant academic research and scientific papers

KRAS G12C INHIBITORS

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Page/Page column 47, (2021/06/22)

The present invention provides compounds of the formula: where R1, R2, R3, R4, R5, A, B, and Y are as described herein, pharmaceutically acceptable salts thereof, and methods of using these compounds and salts for treating patients for cancer.

PENTACYCLIC OXEPINES AND DERIVATIVES THEREOF, COMPOSITIONS AND METHODS

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Page 41, (2010/11/30)

The present invention provides a compound of the formula (I) wherein R1 is -H, -OH, -O(C1-C4 alkyl), -OCOC6H5, -OCO(C1-C6 alkyl), or -OSO2(C2-C6 alkyl); R0, R2 and R3 are each independently -H, -OH, -O(C1-C4 alkyl), -OCOC6H5, -OCO(C1-C6 alkyl), -OSO2(C2-C6 alkyl) or halo; R4 is 1-piperidinyl, 1-pyrrolidinyl, methyl-1-pyrrolidinyl, dimethyl-1-pyrrolidinyl, 4-morpholino, dimethylamino, diethylamino, diisopropylamino, or 1-hexamethyleneimino; n is 2 or 3 X is -S- or -HC=CH-; G is -O-, -S-, -SO-, SO2, or -N(R5)-, wherein R5 is -H or C1-C4 alkyl; and Y is -O-, -S-, -NH-, -NMe-, or -CH2-; or a pharmaceutically acceptable salt thereof; pharmaceutical compositions thereof, optionally in combination with estrogen and progestin; methods of inhibiting a disease associated with estrogen deprivation; and methods for inhibiting a disease associated with an aberrant physiological response to endogenous estrogen.

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