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Ethyl N-[(4-dimethylaminophenyl)methylideneamino]carbamate is a complex organic compound with the chemical formula C12H18N2O2. It is a derivative of carbamic acid, featuring a 4-dimethylaminophenyl group connected to the carbamate moiety through a methyleneimine bridge. ethyl N-[(4-dimethylaminophenyl)methylideneamino]carbamate is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as a precursor in the production of certain herbicides. Its structure provides a stable platform for further chemical modifications, making it a valuable intermediate in the development of new compounds with specific biological activities.

6637-63-4

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6637-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6637-63-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6637-63:
(6*6)+(5*6)+(4*3)+(3*7)+(2*6)+(1*3)=114
114 % 10 = 4
So 6637-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N3O2/c1-4-17-12(16)14-13-9-10-5-7-11(8-6-10)15(2)3/h5-9H,4H2,1-3H3,(H,14,16)/b13-9+

6637-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-[[4-(dimethylamino)phenyl]methylideneamino]carbamate

1.2 Other means of identification

Product number -
Other names 4-dimethylaminobenzaldehyde ethoxycarbonylhydrazone

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:6637-63-4 SDS

6637-63-4Downstream Products

6637-63-4Relevant academic research and scientific papers

Synthesis, oxidation and dehydrogenation of cyclic N,O- and N,S-acetals. Part III. [1,2] Transformation of N,O-acetals: 3-Acyl-1,3,4-oxadiazolines

Somogyi, Laszlo

, p. 1235 - 1246 (2008/09/18)

(Chemical Equation Presented) Various aldehyde and ketone acylhydrazones are synthesized and, under acylating conditions, cyclized into 3-acyl-1,3,4-oxadiazolines. The scope and limitations of these cyclizations and the possible side reactions (e.g. formation of the open-chain N,O-acylhydrazinocarbinols) are dissected. For the first time, simple, convenient and efficient dehydrogenations of 3-acyl-1,3,4-oxadiazolines to oxadiazoles by treatment with potassium permanganate, or more conveniently, with ammonium cerium(IV) nitrate (CAN) are presented. CAN oxidation of 2,2-disubstituted 3-acyl-1,3,4-oxadiazolines, as well as that of aldehyde diacylhydrazones (open-chain isomers of 2,5-disubstituted 3-acyl-1,3,4- oxadiazolines) regenerates the parent carbonyl compounds.

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