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21864-76-6

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21864-76-6 Usage

General Description

2-Ethyl-2-methylbutyronitrile, also known as 2-Ethyl-2-methylbutyronitrile or EMN, is a chemical compound with the molecular formula C8H15N. It is a colorless liquid with a faint odor, and it is used as an intermediate in the production of other chemicals. EMN is primarily utilized as a raw material in the synthesis of various agrochemicals, pharmaceuticals, and dyes. It is also used as a solvent in chemical reactions and as a stabilizer in the formulation of certain pesticides. The chemical is considered to have low acute toxicity, but prolonged exposure may cause irritation to the skin, eyes, and respiratory system. Overall, 2-Ethyl-2-methylbutyronitrile plays a vital role in the manufacturing process of many important chemicals in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 21864-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,6 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21864-76:
(7*2)+(6*1)+(5*8)+(4*6)+(3*4)+(2*7)+(1*6)=116
116 % 10 = 6
So 21864-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-4-7(3,5-2)6-8/h4-5H2,1-3H3

21864-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-2-methylbutanenitrile

1.2 Other means of identification

Product number -
Other names 2-ethyl-2-methyl-butanenitrile

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:21864-76-6 SDS

21864-76-6Relevant articles and documents

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Prout,F.S. et al.

, p. 835 - 838 (1960)

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Wanderungstendenzen cyclischer, polycyclischer und methylverzweigter Alkylreste bei der Beckmann-Umlagerung

Langhals, Heinz,Ruechardt, Christoph

, p. 3831 - 3854 (2007/10/02)

The migration aptitudes of polycyclic bridgehead groups, cycloalkyl groups as well as of β-, γ- and δ-branched alkyl groups in the Chapman variant of the Beckmann rearrangement were determined.From these data it is concluded that at transition state 2 the migrating group is not resembling a planarised carbenium ion R+, but rather a pentacoordinated carbonium ion structure.Because only small geometrical changes occur in the migrating group vertical stabilisation of charge at transition state is believed to have significant influence on the migration aptitudes.

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