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Ethyl 2-(4-chlorobenzylidene)hydrazinecarboxylate is a chemical compound with the molecular formula C10H10ClN2O2. It is a derivative of hydrazinecarboxylic acid, featuring a 4-chlorobenzylidene group attached to the hydrazine moiety. ethyl 2-(4-chlorobenzylidene)hydrazinecarboxylate is an organic molecule that can be used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure consists of a benzene ring with a chlorine atom at the para position, a double bond connecting to the hydrazine group, and an ester group attached to the hydrazine's nitrogen atom. The compound is known for its potential reactivity and may be involved in various chemical transformations, making it a valuable building block in organic synthesis.

3206-35-7

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3206-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3206-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3206-35:
(6*3)+(5*2)+(4*0)+(3*6)+(2*3)+(1*5)=57
57 % 10 = 7
So 3206-35-7 is a valid CAS Registry Number.

3206-35-7SDS

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 N-[(4-chlorophenyl)methylideneamino]carbamate

1.2 Other means of identification

Product number -
Other names 4-Chlor-benzaldehyd-(O-carbamoyl-oxim)

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:3206-35-7 SDS

3206-35-7Relevant academic research and scientific papers

Acetylenic Ketones. 8. Synthesis and Spectroscopic Studies of Some Hydrazones

Baddar, Fawzi G.,Al-Hajjar, Farouk H.,El-Rayyes, Nizar R.

, p. 213 - 217 (2007/10/02)

Aroylphenylacetylenes, benzaldehydes, and acetophenones reacted with ethyl and phenyl hydrazinecarboxylates to give the corresponding hydrazone N-carboxylic esters of ω-aroylacetophenone (IIIa-f), benzaldehyde (IXa-f), and acetophenone (IXg-l).UV, IR, and

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