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76935-65-4

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76935-65-4 Usage

Chemical class

Phenethylamines

Core structure

Phenethylamine

Substitution

Three methyl groups at the 2, 4, and 6 positions

Primary use

Psychoactive drug

Effects

Stimulating and mood-enhancing

Additional use

Performance-enhancing drug in sports

Regulatory status

Regulated and restricted in many countries due to potential for abuse and harmful effects on the body.

Check Digit Verification of cas no

The CAS Registry Mumber 76935-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,3 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76935-65:
(7*7)+(6*6)+(5*9)+(4*3)+(3*5)+(2*6)+(1*5)=174
174 % 10 = 4
So 76935-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N/c1-8-6-9(2)11(4-5-12)10(3)7-8/h6-7H,4-5,12H2,1-3H3/p+1

76935-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4,6-trimethylphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names 2,4,6-Trimethyl-1-<2-amino-aethyl>-benzol

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:76935-65-4 SDS

76935-65-4Downstream Products

76935-65-4Relevant articles and documents

Electron transfer reduction of nitriles using SmI2-Et 3N-H2O: Synthetic utility and mechanism

Szostak, Michal,Sautier, Brice,Spain, Malcolm,Procter, David J.

supporting information, p. 1092 - 1095 (2014/03/21)

The first general reduction of nitriles to primary amines under single electron transfer conditions is demonstrated using SmI2 (Kagan's reagent) activated with Lewis bases. The reaction features excellent functional group tolerance and represents an attractive alternative to the use of pyrophoric alkali metal hydrides. Notably, the electron transfer from Sm(II) to CN functional groups generates imidoyl-type radicals from bench stable nitrile precursors.

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