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4-methylcyclohexane-1-carbonitrile is an organic compound with the molecular formula C8H13N. It is a colorless liquid with a density of 0.91 g/cm3 and a boiling point of 220°C. This chemical is a derivative of cyclohexane, featuring a methyl group attached to the cyclohexane ring and a nitrile functional group (C≡N) at the 1-position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is essential to handle 4-methylcyclohexane-1-carbonitrile with care, as it can be toxic and harmful if inhaled or absorbed through the skin.

524048-18-8

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524048-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 524048-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,4,0,4 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 524048-18:
(8*5)+(7*2)+(6*4)+(5*0)+(4*4)+(3*8)+(2*1)+(1*8)=128
128 % 10 = 8
So 524048-18-8 is a valid CAS Registry Number.

524048-18-8SDS

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 4-methylcyclohexanecarbonitrile

1.2 Other means of identification

Product number -
Other names 4-methyl-cyclohexanecarbonitrile

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:524048-18-8 SDS

524048-18-8Relevant academic research and scientific papers

Corresponding amine nitrile and method of manufacturing thereof

-

, (2017/10/22)

The invention relates to a manufacturing method of nitrile. Compared with the prior art, the manufacturing method has the characteristics of significantly reduced using amount of an ammonia source, low environmental pressure, low energy consumption, low production cost, high purity and yield of a nitrile product and the like, and nitrile with a more complex structure can be obtained. The invention also relates to a method for manufacturing corresponding amine from nitrile.

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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