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2-[(1-Methyl-2-phenylethyl)amino]propanenitrile is a complex organic compound with the molecular formula C12H14N2. It is a derivative of propanenitrile, featuring a phenylethylamine side chain. This molecule is characterized by a 2-phenylethyl group attached to the nitrogen atom of a propanenitrile backbone, with a methyl group on the alpha carbon of the phenylethyl chain. The compound is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly in the development of certain drugs. Its structure and properties make it a versatile building block in organic chemistry, though it is important to note that handling and use should be done with caution due to its potential toxicity and reactivity.

3535-04-4

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3535-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3535-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3535-04:
(6*3)+(5*5)+(4*3)+(3*5)+(2*0)+(1*4)=74
74 % 10 = 4
So 3535-04-4 is a valid CAS Registry Number.

3535-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(1-methyl-2-phenylethyl)amino]propanenitrile

1.2 Other means of identification

Product number -
Other names N-(1-Methyl-2-phenyl-aethyl)-alanin-nitril

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

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More Details:3535-04-4 SDS

3535-04-4Relevant academic research and scientific papers

Thermodynamically Controlled 1,3-Asymmetric Induction in an Acyclic System: Equilibration of α-Amino Nitriles Derived from α-Alkylbenzylamines and Aldehydes

Inaba, Takashi,Fujita, Makoto,Ogura, Katsuyuki

, p. 1274 - 1279 (2007/10/02)

Acyclic α-amino nitriles 1, derived from α-alkylbenzylamines 3 and aldehydes 4 via a Strecker-type reaction, readily epimerize in MeOH at the newly emerged asymmetric center α to the cyano group.The equilibrium diastereomeric ratio :

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