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72679-69-7

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72679-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72679-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,7 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72679-69:
(7*7)+(6*2)+(5*6)+(4*7)+(3*9)+(2*6)+(1*9)=167
167 % 10 = 7
So 72679-69-7 is a valid CAS Registry Number.

72679-69-7SDS

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-butyl-isonicotinonitrile

1.2 Other means of identification

Product number -
Other names 2-Butyl-isonicotinonitril

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:72679-69-7 SDS

72679-69-7Downstream Products

72679-69-7Relevant articles and documents

Nucleophilic Character of the Alkyl Radicals. 19. Absolute Rate Constants in the Homolytic Alkylation of Protonated Heteroaromatic Bases by n-Butyl and tert-Butyl Radicals

Citterio, Attilio,Minisci, Francesco,Franchi, Valeria

, p. 4752 - 4757 (2007/10/02)

The rate constants for the homolytic alkylation of protonated heteroaromatic bases (quinoline, pyridine, and 4-cyano-, 4-acetyl-, 4-methyl-, and 4-methoxypyridine) by n-butyl and tert-butyl radicals were measured at 57 deg C by competition of the aromatic addition with the alkyl radical oxidation by Cu2+ salts (for which the rates are known).With the more activated substrates (quinoline and 4-cyano- and 4-acetylpyridine) the tert-butyl radical is significantly more reactive then the n-butyl radical, clearly showing that polar effects are more important than steric and enthalpic effects in determining the reaction rates.The reversibility of the alkylation by the tert-butyl radical is discussed.

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