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2-(5-Bromo-2-chlorophenyl)acetic acid is a chemical compound with the molecular formula C8H5BrClO2. It is an organic compound that features a carboxylic acid group and two halogens, bromine and chlorine, attached to the phenyl ring. 2-(5-Bromo-2-chlorophenyl)acetic acid is known by various scientific identifiers, including 2-(4-Bromo-2-chlorophenyl)acetic acid and 5-Bromo-2-chlorobenzoic acid. The physical properties of 2-(5-Bromo-2-chlorophenyl)acetic acid, such as solubility and melting point, as well as its chemical reactivity, are primarily influenced by the functional groups present. It is commonly utilized in the synthesis of other chemical compounds within the realm of organic chemistry. Due to its potential harmful effects, it is essential to follow proper handling and safety protocols when working with this substance.

177985-34-1

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177985-34-1 Usage

Uses

Used in Organic Chemistry:
2-(5-Bromo-2-chlorophenyl)acetic acid is used as a synthetic intermediate for the preparation of various chemical compounds. Its unique structure, which includes a carboxylic acid group and two halogens, makes it a valuable building block in the synthesis of a wide range of organic molecules.
Used in Pharmaceutical Industry:
2-(5-Bromo-2-chlorophenyl)acetic acid is used as a key component in the development of pharmaceuticals. Its chemical properties allow it to be incorporated into drug molecules, potentially leading to the creation of new therapeutic agents with novel mechanisms of action.
Used in Chemical Research:
2-(5-Bromo-2-chlorophenyl)acetic acid is employed as a research tool in chemical studies. Its reactivity and structural features make it an interesting subject for investigations into reaction mechanisms, synthetic strategies, and the exploration of new chemical space.
Used in Material Science:
2-(5-Bromo-2-chlorophenyl)acetic acid is used as a precursor in the development of new materials. Its incorporation into polymers or other materials can lead to the creation of novel materials with unique properties, such as improved stability, enhanced reactivity, or altered physical characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 177985-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,9,8 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 177985-34:
(8*1)+(7*7)+(6*7)+(5*9)+(4*8)+(3*5)+(2*3)+(1*4)=201
201 % 10 = 1
So 177985-34-1 is a valid CAS Registry Number.

177985-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-bromo-2-chlorophenyl)acetic acid

1.2 Other means of identification

Product number -
Other names Benzeneacetic acid,5-bromo-2-chloro

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:177985-34-1 SDS

177985-34-1Relevant articles and documents

NOVEL 2-AMINO-PYRIDINE AND 2-AMINO-PYRIMIDINE DERIVATIVES AND MEDICINAL USE THEREOF

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Paragraph 0479, (2017/03/14)

Provided is a compound superior in an autotaxin inhibitory action and the like, effective as a prophylactic or therapeutic drug for diseases involving ATX. The present invention relates to a compound represented by the following formula (I): [wherein each symbol is as described in the DESCRIPTION], which has a superior autotaxin inhibitory action and is useful as a prophylactic or therapeutic drug for diseases involving ATX.

2- and 2,5-substituted phenylketoenols

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Page column 80, (2010/01/31)

The invention relates to novel phenyl-substituted cyclic ketoenols of the formula (I) in which Het represents one of the groups ?in which A, B, D, G, X and Z are each as defined in the description, to a plurality of processes and intermediates for their preparation, and to their use as pesticides.

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