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710-40-7

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710-40-7 Usage

Chemical compound

5-hexyl-2-methylpyridine

Class

Pyridine derivative

Primary use

Flavoring agent in the food industry

Natural sources

Coffee, cocoa, roasted peanuts

Properties

Insect-repelling

Uses

Formulation of insecticides and pest control products

Studies

Potential pharmacological activities and biological processes

Safety profile

Not extensively documented

Research needed

To fully understand properties and applications

Check Digit Verification of cas no

The CAS Registry Mumber 710-40-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 710-40:
(5*7)+(4*1)+(3*0)+(2*4)+(1*0)=47
47 % 10 = 7
So 710-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H19N/c1-3-4-5-6-7-12-9-8-11(2)13-10-12/h8-10H,3-7H2,1-2H3

710-40-7SDS

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 5-Hexyl-2-methylpyridine

1.2 Other means of identification

Product number -
Other names Pyridine,5-hexyl-2-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:710-40-7 SDS

710-40-7Downstream Products

710-40-7Relevant articles and documents

DIELS-ALDER REACTION OF 1,2,3-TRIAZINE WITH ALDEHYDE ENAMINE

Koyama, Junko,Ogura, Tamaki,Tagahara, Kiyoshi

, p. 1595 - 1600 (2007/10/02)

The Diels-Alder reaction of 4-methyl-1,2,3-triazine with several aldehyde enamines was carried out to afford 2,5-disubstituted pyridines.As an application of this method, we accomplished the synthesis of alkaloid, fusaric acid.

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