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3-METHYLVALERONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21101-88-2

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21101-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21101-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,0 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21101-88:
(7*2)+(6*1)+(5*1)+(4*0)+(3*1)+(2*8)+(1*8)=52
52 % 10 = 2
So 21101-88-2 is a valid CAS Registry Number.

21101-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylpentanenitrile

1.2 Other means of identification

Product number -
Other names Pentanenitrile,3-methyl

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:21101-88-2 SDS

21101-88-2Relevant articles and documents

Corresponding amine nitrile and method of manufacturing thereof

-

, (2018/05/07)

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.

Highly practical synthesis of nitriles and heterocycles from alcohols under mild conditions by aerobic double dehydrogenative catalysis

Yin, Weiyu,Wang, Chengming,Huang, Yong

supporting information, p. 1850 - 1853 (2013/06/04)

A mild, aerobic, catalytic process for obtaining nitriles directly from alcohols and aqueous ammonia is described. The reaction proceeds via a dehydrogenation cascade mediated by catalytic CuI, bpy, and TEMPO in the presence of O2. The substrate scope is broad including various functionalized aromatic and aliphatic alcohols. This protocol enabled the one-pot synthesis of various biaryl heterocycles directly from commercially available alcohols.

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