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2-cyclohexylcyclopropanecarboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91056-79-0

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91056-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91056-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,5 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91056-79:
(7*9)+(6*1)+(5*0)+(4*5)+(3*6)+(2*7)+(1*9)=130
130 % 10 = 0
So 91056-79-0 is a valid CAS Registry Number.

91056-79-0SDS

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 (1SR,2RS)-2-cyclohexylcyclopropanecarboxylic acid

1.2 Other means of identification

Product number -
Other names (1S,2R)-2-Cyclohexyl-cyclopropanecarboxylic 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:91056-79-0 SDS

91056-79-0Relevant academic research and scientific papers

Modular Access to Substituted Azocanes via a Rhodium-Catalyzed Cycloaddition-Fragmentation Strategy

Shaw, Megan H.,Croft, Rosemary A.,Whittingham, William G.,Bower, John F.

, p. 8054 - 8057 (2015/07/15)

A short entry to substituted azocanes by a Rh-catalyzed cycloaddition-fragmentation process is described. Specifically, exposure of diverse N-cyclopropylacrylamides to phosphine-ligated cationic Rh(I) catalyst systems under a CO atmosphere enables the directed generation of rhodacyclopentanone intermediates. Subsequent insertion of the alkene component is followed by fragmentation to give the heterocyclic target. Stereochemical studies show, for the first time, that alkene insertion into rhodacyclopentanones can be reversible.

Structure-based design and synthesis of potent benzothiazole inhibitors of interleukin-2 inducible T cell kinase (ITK)

Mackinnon, Colin H.,Lau, Kevin,Burch, Jason D.,Chen, Yuan,Dines, Jonathon,Ding, Xiao,Eigenbrot, Charles,Heifetz, Alexander,Jaochico, Allan,Johnson, Adam,Kraemer, Joachim,Kruger, Susanne,Krülle, Thomas M.,Liimatta, Marya,Ly, Justin,Maghames, Rosemary,Montalbetti, Christian A.G.N.,Ortwine, Daniel F.,Pérez-Fuertes, Yolanda,Shia, Steven,Stein, Daniel B.,Trani, Giancarlo,Vaidya, Darshan G.,Wang, Xiaolu,Bromidge, Steven M.,Wu, Lawren C.,Pei, Zhonghua

, p. 6331 - 6335 (2013/11/19)

Inhibition of the non-receptor tyrosine kinase ITK, a component of the T-cell receptor signalling cascade, may represent a novel treatment for allergic asthma. Here we report the structure-based optimization of a series of benzothiazole amides that demons

1,4-disubstituted benzo-fused cycloalkyl urea compounds

-

, (2015/04/15)

Disclosed are compounds of the formula (I) shown below which are active as anti-inflammatory agents. Also disclosed are methods of using and making such compounds. wherein n, X, A, L, J, p, Q, Y and z are described herein.

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