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

19424-34-1

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19424-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19424-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,2 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19424-34:
(7*1)+(6*9)+(5*4)+(4*2)+(3*4)+(2*3)+(1*4)=111
111 % 10 = 1
So 19424-34-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-7(2)5-3-4-6-8/h7H,3-5H2,1-2H3

19424-34-1SDS

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-METHYLHEXANENITRILE

1.2 Other means of identification

Product number -
Other names 5-Methyl-hexannitril

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:19424-34-1 SDS

19424-34-1Downstream Products

19424-34-1Relevant articles and documents

A New Facile Route to Primary Alkanenitriles from Terminal Alkenes via a Hydroboration-Cyanation Sequence

Masuda, Yuzuru,Hoshi, Masayuki,Arase, Akira

, p. 266 - 267 (1989)

Terminal alkenes are converted into one-carbon homologated primary alkanenitriles in high yields via hydroboration followed by a reaction with copper(I) cyanide, copper(II) acetate, and copper(II) acetylacetonate.

Chemoenzymatic synthesis of a series of 4-substituted glutamate analogues and pharmacological characterization at human glutamate transporters subtypes 1-3

Alaux, Sebastien,Kusk, Mie,Sagot, Emanuelle,Bolte, Jean,Jensen, Anders A.,Br?uner-Osborne, Hans,Gefflaut, Thierry,Bunch, Lennart

, p. 7980 - 7992 (2007/10/03)

A series of nine L-2,4-s;yrc-4-alkylglutamic acid analogues (1a-i) were synthesized in high yield and high enantiomeric excess (>99% ee) from their corresponding 4-substituted ketoglutaric acids (2a-i), using the enzyme aspartate aminotransferase (AAT) from pig heart or E. coli. The synthesized compounds were evaluated as potential ligands for the glutamate transporters EAAT1, EAAT2, and EAAT3 (excitatory amino acid transporter, subtypes 1-3) in the FLIPR membrane potential (FMP) assay. We found a distinct change in the pharmacological profile when the 4-methyl group (compound 1a, an EAAT1 substrate and EAAT2,3 inhibitor) was extended to a 4-ethyl group, compound 1b, as this analogue is an inhibitor at all three subtypes, EAAT1-3. Furthermore, we conclude that both large and bulky hydrophobic substituents in the 4-position of L-2,4-syn Glu are allowed by all three glutamate transporter subtypes EAAT1-3 while maintaining inhibitory activity.

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