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34579-77-6

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34579-77-6 Usage

Functional group

Nitrile (carbon-triple bond with nitrogen)

Physical state

Colorless liquid

Uses

Solvent in pharmaceutical and chemical industries, intermediate in the production of other chemicals (including pesticides and pharmaceuticals), potential monomer for the synthesis of various polymers

Hazards

Can cause irritation to skin, eyes, and respiratory system upon exposure

Check Digit Verification of cas no

The CAS Registry Mumber 34579-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,7 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34579-77:
(7*3)+(6*4)+(5*5)+(4*7)+(3*9)+(2*7)+(1*7)=146
146 % 10 = 6
So 34579-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H15N/c1-4-8(5-2,6-3)7-9/h4-6H2,1-3H3

34579-77-6SDS

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 2,2-diethylbutanenitrile

1.2 Other means of identification

Product number -
Other names 2,2-Diethyl-butyronitril

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:34579-77-6 SDS

34579-77-6Relevant articles and documents

Limitations on the Persistence of Iminoxyls: Isolation of tert-Butyl 1,1-Diethylpropyl Ketiminoxyl and Related Radicals

Eisenhauer, Brian M.,Wang, Minghui,Labaziewicz, Henryk,Ngo, Maria,Mendenhall, G. David

, p. 2050 - 2053 (2007/10/03)

A series of iminoxyl radicals of the general formula R(C=NO?)R1, with R and R1 usually tertiary, was synthesized in a search for radicals of increased persistence. Three new radicals were isolated as blue liquids: Et3C(C=NO?)Bu-t (1), t-C5H11(C=NO?)Bu-t (2), and (t-C5H11)2C=NO? (3). Oxidation of oximes Et3C(C=NOH)Ph (4H), PhCH2CMe2(C=NOH)Bu-t (5H), PhCMe2(C=NOH)Bu-t (6H), and Me2CH(C=NOH)C5H11-t (7H), among others, did not lead to isolable iminoxyls. A new, convenient synthesis of symmetrical tertiary imines from tert-RCl, tert-RCN, and Na is described. Radical t-Bu2C=NO? (8) and cyclohexene readily gave the allylic substitution product, 2,2,4,4-tetramethyl- 3-hexanone O-(2′-cyclohexen-1′-yl)oxime.

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