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10278-71-4

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10278-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10278-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,7 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10278-71:
(7*1)+(6*0)+(5*2)+(4*7)+(3*8)+(2*7)+(1*1)=84
84 % 10 = 4
So 10278-71-4 is a valid CAS Registry Number.

10278-71-4SDS

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 N,N-dimethyl-N'-(2-methylphenyl)methanimidamide

1.2 Other means of identification

Product number -
Other names N1N1-dimethyl-N2-ortho-methylphenylformamidine

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:10278-71-4 SDS

10278-71-4Downstream Products

10278-71-4Relevant articles and documents

Reactions of dimethylammonium Chloride with Methyl Ketones, Primary Amines, and Unsubstituted Amides

Gupton, John T.,Colon, Cesar,Harrison, Charles R.,Lizzi, Michael J.,Polk, Dale E.

, p. 4522 - 4524 (1980)

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A Versatile New Synthesis of Quinolines and Related Fused Pyridines. Part 5. The Synthesis of 2-Chloroquinoline-3-carbaldehydes

Meth-Cohn, Otto,Narine, Bramha,Tarnowski, Brian

, p. 1520 - 1530 (2007/10/02)

Acetanilides are converted into 2-chloroquinoline-3-carbaldehydes in good yield by the action of Vilsmeier's reagent in phosphoryl chloride solution.The reaction is shown to involve successive conversion of the acetanilide into an imidoyl chloride and then an N-(α-chlorovinyl)aniline.The latter enamine is diformylated at its β-position and subsequently cyclised to the chloroquinolinecarbaldehyde.The diformylated intermediates may be isolated in several cases and separately cyclised with polyphosphoric acid.

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