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53663-29-9

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53663-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53663-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,6 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53663-29:
(7*5)+(6*3)+(5*6)+(4*6)+(3*3)+(2*2)+(1*9)=129
129 % 10 = 9
So 53663-29-9 is a valid CAS Registry Number.

53663-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyldodec-2-enoic acid

1.2 Other means of identification

Product number -
Other names 2-methyl-dodec-2t-enoic acid

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:53663-29-9 SDS

53663-29-9Relevant articles and documents

Highly potent, orally available anti-inflammatory broad-spectrum chemokine inhibitors

Fox, David J.,Reckless, Jill,Lingard, Hannah,Warren, Stuart,Grainger, David J.

supporting information; experimental part, p. 3591 - 3595 (2010/03/30)

A series of 3-acylaminocaprolactams are inhibitors of chemokine-induced chemotaxis. Branching of the side chain α-carbon provides highly potent inhibitors of a range of CC and CXC chemokines. The most potent compound has an ED50 of 40 pM. Selec

Phosphite-Mediated in Situ Carboxyvinylation: A New General Acrylic Acid Synthesis

Brittelli, David R.

, p. 2514 - 2520 (2007/10/02)

Sequential treatment of a 2-halo carboxylic acid with a dialkyl phosphite and an aldehyde or ketone in the presence of 3 equiv of sodium hydride in glyme constitutes a new general acrylic acid synthesis superior to conventional methods.An alkoxide-in-alcohol variant may be used with bromo- or chloroacetic acid and aryl aldehydes to produce cinnamic acids conveniently.The scope and other features of the synthesis are discussed.

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