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5335-36-4

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5335-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5335-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5335-36:
(6*5)+(5*3)+(4*3)+(3*5)+(2*3)+(1*6)=84
84 % 10 = 4
So 5335-36-4 is a valid CAS Registry Number.

5335-36-4SDS

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 ethyl (2Z)-2-cyano-2-(phenylhydrazinylidene)acetate

1.2 Other means of identification

Product number -
Other names Cyan-phenylhydrazono-essigsaeure-aethylester

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:5335-36-4 SDS

5335-36-4Relevant articles and documents

Reaction of (chloro carbonyl) phenyl ketene with 5-amino pyrazolones: Synthesis, characterization and theoretical studies of 7-hydroxy-6-phenyl-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-2,5(1H,4H)-dione derivatives

Zahedifar, Mahboobeh,Razavi, Razieh,Sheibani, Hassan

, p. 730 - 735 (2016/07/26)

New 7-hydroxy-6-phenyl-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-2,5(1H,4H)-dione derivatives were synthesized from the reaction of (chlorocarbonyl)phenyl ketene and 5-amino pyrazolones in high to excellent yields and short reaction times. Structures of

Voltammetric Studies on Some Arylhydrazones of α-Cyano Ketones and α-Cyano Esters

Abou-Elenien, G. M.,Ismail, N. A.,Hafez, T. S.

, p. 651 - 654 (2007/10/02)

The redox characteristics of the title compounds are extensively studied using DC-, cyclic voltammetry, coulometry, and controlled potential electrolysis in benzonitrile at platinum electrodes.These compounds are oxidized in one-electron transfer process followed by deprotonation which leads to dimerization.The reduction process differs according to the nature of the compound and the electron-withdrawing power of the substituent in the α-position.They can be reduced in a single two electron or two one electron waves leading in both cases to saturation of the hydrazonic moiety.

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