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Cyclohexanecarbonitrile, 2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90154-71-5

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90154-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90154-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,5 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90154-71:
(7*9)+(6*0)+(5*1)+(4*5)+(3*4)+(2*7)+(1*1)=115
115 % 10 = 5
So 90154-71-5 is a valid CAS Registry Number.

90154-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylcyclohexane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-methylcyclohexanecarbonitrile

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:90154-71-5 SDS

90154-71-5Relevant academic research and scientific papers

METHOD FOR PRODUCING NITRILE COMPOUND

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Paragraph 0041-0044; 0048; 0051, (2016/11/17)

PROBLEM TO BE SOLVED: To provide a method for producing a nitrile compound capable of obtaining a nitrile compound in a short time and at a low temperature, while maintaining a high yield. SOLUTION: There is provided a method for producing a nitrile compound using a compound having a hydroxymethylene group as a raw material. The nitrile compound is obtained by mixing and reacting an aliphatic compound or an aromatic compound having a hydroxymethylene group with a N-nitrosyl compound, an oxidant, an iodinating agent and ammonia water. COPYRIGHT: (C)2015,JPO&INPIT

Cyclohexylcarbonitriles: Diastereoselective arylations with TMPZnCl·LiCl

Mycka, Robert J.,Duez, Stephanie,Bernhardt, Sebastian,Heppekausen, Johannes,Knochel, Paul,Fleming, Fraser F.

, p. 7671 - 7676 (2012/10/30)

Deprotonating substituted cyclohexanecarbonitriles with TMPZnCl·LiCl affords zincated nitriles that diastereoselectively couple with aryl bromides in the presence of catalytic Pd(OAc)2 and S-Phos. Steric and electronic effects influence the dia

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