202001-01-2 Usage
Uses
Used in Pharmaceutical Research:
(3-bromo-5-chloro-phenyl)-acetic acid is utilized as a building block in the creation of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs.
Used in Organic Synthesis:
In the field of organic chemistry, (3-bromo-5-chloro-phenyl)-acetic acid is employed as an intermediate for synthesizing a range of organic compounds, contributing to the diversity of chemical products.
Used in Anti-inflammatory Applications:
(3-bromo-5-chloro-phenyl)-acetic acid may serve as an anti-inflammatory agent, potentially offering therapeutic benefits for conditions characterized by inflammation.
Used in Antimicrobial Applications:
Possessing antimicrobial properties, (3-bromo-5-chloro-phenyl)-acetic acid could be used to combat microbial infections, providing an alternative in the treatment of various diseases.
Used in Agrochemical Development:
This chemical may also be employed in the development of agrochemicals, contributing to the creation of pesticides or other agricultural products to enhance crop protection and yield.
Used in Specialized Materials:
(3-bromo-5-chloro-phenyl)-acetic acid's versatility extends to the development of specialized materials for specific industrial applications, showcasing its broad utility in material sciences.
Check Digit Verification of cas no
The CAS Registry Mumber 202001-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,0,0 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 202001-01:
(8*2)+(7*0)+(6*2)+(5*0)+(4*0)+(3*1)+(2*0)+(1*1)=32
32 % 10 = 2
So 202001-01-2 is a valid CAS Registry Number.
202001-01-2Relevant articles and documents
PPAR ACTIVE COMPOUNDS
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Page/Page column 66; 67, (2008/12/08)
Compounds are described that are active on at least one of PPARα, PPARδ, and PPARγ, which are useful for therapeutic and/or prophylactic methods involving modulation of at least one of PPARα, PPARδ, and PPARγ.
Synthesis of dihalophenylacetic acids using aromatic nucleophilic substitution strategy
Kowalczyk, Bruce A.
, p. 1411 - 1414 (2007/10/03)
A simple synthetic strategy to dihalophenylacetic acids and specifically 3,5-difluorophenylacetic acid an important pharmaceutical intermediate was developed. The aromatic nucleophilic substitution of dihalofluorobenzenes using the anion of ethyl cyanoacetate yielded ethyl dihalophenylcyanoacetates. The basic decarboxylation of the ethyl dihalophenylcyanoacetates produced targeted dihalophenylacetic acids.
