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Cyclohexanecarboxylic acid, 5-methyl-2-(1-methylethyl)-, 2-(2-hydroxyethoxy)ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57233-20-2

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57233-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57233-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,3 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57233-20:
(7*5)+(6*7)+(5*2)+(4*3)+(3*3)+(2*2)+(1*0)=112
112 % 10 = 2
So 57233-20-2 is a valid CAS Registry Number.

57233-20-2SDS

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-(2'-hydroxyethoxy)-ethyl p-menthane-3-carboxylate

1.2 Other means of identification

Product number -
Other names 2-(2'-Hydroxyethoxy)Ethyl p-Menthane 3-Carboxylate

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:57233-20-2 SDS

57233-20-2Downstream Products

57233-20-2Relevant academic research and scientific papers

Aryl-substituted derivatives of cycloalkyl and branched chain alkyl carboxylic acids useful as antinociceptive drugs for peripheral targets

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Page/Page column 8, (2008/06/13)

Novel peripheral antinociceptive compounds are disclosed having a pharmacophore unit that target small-diameter nerve fibers that transmit signals of pain and discomfort from the soma and viscera. By acting on this target, the pharmacophore unit obtunds pain and diminishes hyper-reflexia from organs such as the skin, the respiratory tract, the corpus, the lower urinary tract, and the bowel. The pharmacophore unit is coupled to substituents that facilitate delivery of the pharmacophore to its target.

Substituted p-menthanes

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, (2008/06/13)

Compounds are disclosed having a physiological cooling action on the skin. The compositions contain, as the effective ingredient, certain esters of p-menthane 3-carboxylic acid.

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