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N-Cyanomethyl-2-ethylanilin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60394-62-9

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60394-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60394-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,9 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60394-62:
(7*6)+(6*0)+(5*3)+(4*9)+(3*4)+(2*6)+(1*2)=119
119 % 10 = 9
So 60394-62-9 is a valid CAS Registry Number.

60394-62-9SDS

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 N-Cyanomethyl-2-ethylanilin

1.2 Other means of identification

Product number -
Other names -

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:60394-62-9 SDS

60394-62-9Relevant academic research and scientific papers

Iron-catalyzed reductive strecker reaction

Yan, Fachao,Huang, Zijun,Du, Chen-Xia,Bai, Jian-Fei,Li, Yuehui

, p. 188 - 194 (2021/02/03)

Strecker reaction is widely applied for the synthesis of amino acids from aldehydes, amines and cyanides. Herein, we report the FeI2-catalyzed reductive Strecker type reaction of formamides instead of aldehydes to produce amino acetonitriles. The challenging capture of carbinolamine intermediates by CN? was achieved via Fe catalysis. This approach afforded better yields than the use of Ir- or Rh-catalysts. The application ability of this methodology is demonstrated by 1) one-pot construction of (13C labeled) complex molecules from CO2 via amino acetonitrile intermediates and 2) convenient production of homologated carboxylic acids from aldehydes.

2-Chloro-N-(cyanomethyl)acetanilides

-

, (2008/06/13)

A series of 2-chloro-N-(cyanomethyl)acetanilide compounds are active as selective herbicides for protecting certain crops against infestation by undesirable grasses.

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