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109458-85-7

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109458-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109458-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,5 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 109458-85:
(8*1)+(7*0)+(6*9)+(5*4)+(4*5)+(3*8)+(2*8)+(1*5)=147
147 % 10 = 7
So 109458-85-7 is a valid CAS Registry Number.

109458-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-1-methylcyclohex-1-ene

1.2 Other means of identification

Product number -
Other names .3-Chlor-1-methyl-cyclohexen

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:109458-85-7 SDS

109458-85-7Relevant articles and documents

New routes to ss-cycloalkylalanine derivatives using serine-derived organozinc reagents

Carrillo-Marquez, Tomas,Caggiano, Lorenzo,Jackson, Richard F. W.,Grabowska, Urszula,Rae, Alastair,Tozer, Matthew J.

, p. 4117 - 4123 (2005)

Two distinct routes to β-cycloalkylalanine derivatives have been developed. The first route employs the reaction of the iodoalanine-derived zinc-copper reagent 2 with cycloalk-l-en-3-yl phosphates, and the second uses the palladium-catalysed coupling of t

TRIAZOLYL DERIVATIVES AS SYK INHIBITORS

-

Page/Page column 104, (2014/04/17)

Provided are triazole derivatives of Formula I which are potent inhibitors of spleen tyrosine kinase and pharmaceutical composition. The triazole derivatives are useful in the treatment and prevention of diseases mediated by said enzyme, such as asthma, COPD, rheumatoid arthritis, and cancer.

Mild two-step process for the transition-metal-free synthesis of carbon-carbon bonds from allylic alcohols/ethers and grignard reagents

Han, Xinping,Zhang, Yanhua,Wu, Jimmy

supporting information; experimental part, p. 4104 - 4106 (2010/05/15)

Chemical Equation Represented A mild two-step process for the regioselective, transition-metal-free preparation of carbon-carbon bonds from allylic alcohols/ethers and Grignard reagents is described. This process obviates the need for the harsh deprotecti

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