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240490-00-0

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240490-00-0 Usage

General Description

AMINO-(2-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID is a chemical compound with the molecular formula C9H9F3NO2. It is an amino acid derivative with a trifluoromethyl-phenyl group attached to the acetic acid backbone. AMINO-(2-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID is used in the pharmaceutical industry for the synthesis of potential drug candidates and in medicinal chemistry research. It has various biological activities and is being studied for its potential therapeutic applications in the treatment of various diseases. Its unique chemical structure and properties make it a valuable compound for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 240490-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,4,9 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 240490-00:
(8*2)+(7*4)+(6*0)+(5*4)+(4*9)+(3*0)+(2*0)+(1*0)=100
100 % 10 = 0
So 240490-00-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H8F3NO2/c10-9(11,12)6-4-2-1-3-5(6)7(13)8(14)15/h1-4,7H,13H2,(H,14,15)/t7-/m0/s1

240490-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-2-[2-(trifluoromethyl)phenyl]acetic acid

1.2 Other means of identification

Product number -
Other names -

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:240490-00-0 SDS

240490-00-0Upstream product

240490-00-0Downstream Products

240490-00-0Relevant articles and documents

Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine

Inada, Haruki,Shibuya, Masatoshi,Yamamoto, Yoshihiko

, p. 11047 - 11059 (2020/10/12)

The transamination of α-keto acids with 2-phenylglycine is an effective methodology for directly synthesizing unprotected α-amino acids. However, the synthesis of 2-arylglycines by transamination is problematic because the corresponding products, 2-arylglycines, transaminate the starting arylglyoxylic acids. Herein, we demonstrate the use of commercially available l-2-(2-chlorophenyl)glycine as the nitrogen source in the transamination of arylglyoxylic acids, producing the corresponding 2-arylglycines without interference from the undesired self-transamination process.

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