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313490-25-4

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313490-25-4 Usage

General Description

Tert-butoxycarbonylamino-(2-chloro-phenyl)-acetic acid is a chemical compound with the molecular formula C12H15ClNO4. It is commonly used in the synthesis of pharmaceuticals and other organic compounds. This chemical has the potential to act as a prodrug, meaning it could be metabolized in the body to produce the active form of the drug. It is also known for its ability to inhibit certain enzymes and has been studied for its potential use in treating various medical conditions. Overall, tert-butoxycarbonylamino-(2-chloro-phenyl)-acetic acid has potential therapeutic applications and is of interest for further research in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 313490-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,4,9 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 313490-25:
(8*3)+(7*1)+(6*3)+(5*4)+(4*9)+(3*0)+(2*2)+(1*5)=114
114 % 10 = 4
So 313490-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H16ClNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-6-4-5-7-9(8)14/h4-7,10H,1-3H3,(H,15,18)(H,16,17)

313490-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chlorophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]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:313490-25-4 SDS

313490-25-4Relevant articles and documents

Chemo-enzymatic approach to the synthesis of the antithrombotic clopidogrel

Ferraboschi, Patrizia,Mieri, Maria De,Galimberti, Fiorella

, p. 2136 - 2141 (2010)

The (S)-2-chlorophenylglycine moiety is well recognized in the structure of (S)-clopidogrel, a known antithrombotic drug. We prepared an enantiomerically pure chiral building block via an enzyme-catalyzed resolution of (RS)-N-Boc-2-chlorophenylglycine methylester. The best results were obtained by means of an immobilized subtilisin, the cross-linked enzyme aggregate (Alcalase-CLEA). The high enantiomeric excess of the synthon obtained remained the same over the course of clopidogrel synthesis; the simplicity of the process makes this pathway suitable for large-scale preparation.

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