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192725-73-8

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192725-73-8 Usage

Uses

Different sources of media describe the Uses of 192725-73-8 differently. You can refer to the following data:
1. 3-(2,6-Dimethylphenyl)propionic acid is used in the preparation of peptide analogs as retroviral protease inhibitors for inhibiting HIV infection
2. It is used in the preparation of peptide analogs as retroviral protease inhibitors for inhibiting HIV infection.

Check Digit Verification of cas no

The CAS Registry Mumber 192725-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,7,2 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 192725-73:
(8*1)+(7*9)+(6*2)+(5*7)+(4*2)+(3*5)+(2*7)+(1*3)=158
158 % 10 = 8
So 192725-73-8 is a valid CAS Registry Number.

192725-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,6-dimethylphenyl)propanoic 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:192725-73-8 SDS

192725-73-8Relevant articles and documents

Rhodium(I)-catalyzed 1,4-addition of arylboronic acids to acrylic acid in water: One-step preparation of 3-arylpropionic acids

Vautravers, Nicolas R.,Breit, Bernhard

supporting information; experimental part, p. 2517 - 2520 (2011/11/12)

A practical method for the one-step preparation of 3-arylpropionic acids through rhodium-catalyzed 1,4-addition of arylboronic acids to acrylic acid is reported. The method is applicable to a broad scope of aryl boronic acids and displays a wide functional group tolerance operating in water as the optimal reaction medium. Georg Thieme Verlag Stuttgart · New York.

Retroviral protease inhibiting compounds

-

Page 52, (2010/01/31)

A compound comprising a substituent of the formula (II) is disclosed as an HIV protease inhibitor. Intermediates for making such compounds and processes for making such intermediates are also disclosed.

RETROVIRAL PROTEASE INHIBITING COMPOUNDS

-

, (2008/06/13)

A compound of the formula: STR1 is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.

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