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Diethyl 1-(cyclohexa-2,4-dien-1-yl)hydrazine-1,2-dicarboxylate is a complex organic compound with the chemical formula C12H18N2O4. It is a derivative of hydrazine, featuring a cyclohexa-2,4-dien-1-yl group attached to the hydrazine moiety. diethyl 1-(cyclohexa-2,4-dien-1-yl)hydrazine-1,2-dicarboxylate is characterized by its two ester groups, which are derived from dicarboxylic acid, and are connected to the nitrogen atoms of the hydrazine. It is a colorless to pale yellow liquid and is soluble in organic solvents. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Due to its reactivity and potential toxicity, it is important to handle diethyl 1-(cyclohexa-2,4-dien-1-yl)hydrazine-1,2-dicarboxylate with care, following appropriate safety protocols.

7355-78-4

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7355-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7355-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7355-78:
(6*7)+(5*3)+(4*5)+(3*5)+(2*7)+(1*8)=114
114 % 10 = 4
So 7355-78-4 is a valid CAS Registry Number.

7355-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-cyclohexa-2,4-dien-1-yl-N-(ethoxycarbonylamino)carbamate

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

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More Details:7355-78-4 SDS

7355-78-4Downstream Products

7355-78-4Relevant academic research and scientific papers

Anatomy of Ene and Diels-Alder Reactions between Cyclohexadienes and Azodicarboxylates

Jenner, Gerard,Salem, Ridha Ben

, p. 1961 - 1964 (2007/10/02)

In contrast with other (C...H...N) hydrogen transfers, the high-pressure kinetics of the ene reaction between cyclohexa-1,4-diene and diethyl azodicarboxylate show a concerted transition state.The discrepancy is assingned to the enhanced rigidity of the cyclohexadiene molecule with orthogonal hydrogen transfer to the nitrogen atom.Cyclohexa-1,3-diene reacts with diethyl azodicarboxylate according to a concerted Diels-Alder reaction.

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