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21478-01-3

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  • Hexadecanoic acid,2-[(dichloroacetyl)amino]-3-hydroxy-3-[4-(methylsulfonyl)phenyl]propyl ester,[R-(R*,R*)]- (9CI)

    Cas No: 21478-01-3

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21478-01-3 Usage

General Description

[R-(R*,R*)]-2-[(dichloroacetyl)amino]-3-hydroxy-3-[4-(methylsulphonyl)phenyl]propyl palmitate is a chemical compound that falls under the category of palmitate esters. It is a derivative of palmitic acid and is used in pharmaceutical products as an anti-inflammatory and analgesic agent. The compound contains a dichloroacetyl group, a hydroxy group, and a methylsulphonylphenyl group, all of which contribute to its pharmacological properties. This chemical has potential therapeutic applications in the treatment of various inflammatory and pain-related conditions. However, it is important to note that the compound should be handled and used with caution due to its potential hazardous nature.

Check Digit Verification of cas no

The CAS Registry Mumber 21478-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,7 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21478-01:
(7*2)+(6*1)+(5*4)+(4*7)+(3*8)+(2*0)+(1*1)=93
93 % 10 = 3
So 21478-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C28H45Cl2NO6S/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-25(32)37-21-24(31-28(34)27(29)30)26(33)22-17-19-23(20-18-22)38(2,35)36/h17-20,24,26-27,33H,3-16,21H2,1-2H3,(H,31,34)

21478-01-3SDS

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 threo-(1R,2R)-1-<(4-methylsulfonyl)phenyl>-2-(dichloroacetamido)-1,3-propanediol 3-palmitate

1.2 Other means of identification

Product number -
Other names Hexadecanoic acid (2R,3R)-2-(2,2-dichloro-acetylamino)-3-hydroxy-3-(4-methanesulfonyl-phenyl)-propyl ester

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:21478-01-3 SDS

21478-01-3Downstream Products

21478-01-3Relevant articles and documents

Regioselective preparation of thiamphenicol esters through lipase-catalyzed processes

Da Silva, Marcos R.,Montenegro, Tasso G.C.,De Mattos, Marcos C.,De Oliveira, Maria Da Conceic?a?o F.,De Lemos, Telma L.G.,De Gonzalo, Gonzalo,Lavandera, Iva?n,Gotor-Ferna?ndez, Vicente,Gotor, Vicente

, p. 987 - 994 (2014/07/07)

The lipase-catalyzed synthesis of thiamphenicol derivatives has been studied through complementary acylation and hydrolytic approaches, finding Candida antarctica lipase B as the most efficient biocatalyst for the selective modification of both thiampheni

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