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2-Cyclopenten-1-one (2,4-dinitrophenyl)hydrazone is a chemical compound with the molecular formula C11H10N4O4. It is a derivative of cyclopentenone, featuring a hydrazone functional group formed by the reaction of 2-cyclopenten-1-one with 2,4-dinitrophenylhydrazine. This yellow crystalline solid is known for its potential applications in organic synthesis and as a reagent in chemical analysis. The compound exhibits a molecular weight of 258.22 g/mol and has a melting point of approximately 198-200°C. Its chemical structure is characterized by a cyclopentenone ring with a 2,4-dinitrophenyl group attached to the nitrogen atom of the hydrazone moiety. Due to the presence of nitro groups, 2-Cyclopenten-1-one (2,4-dinitrophenyl)hydrazone may possess explosive properties and should be handled with caution.

789-99-1

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789-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 789-99-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 789-99:
(5*7)+(4*8)+(3*9)+(2*9)+(1*9)=121
121 % 10 = 1
So 789-99-1 is a valid CAS Registry Number.

789-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopent-2-enone-(2,4-dinitro-phenylhydrazone)

1.2 Other means of identification

Product number -
Other names Cyclopenten-(1)-on-(3)-(2,4-dinitro-phenylhydrazon)

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:789-99-1 SDS

789-99-1Downstream Products

789-99-1Relevant articles and documents

Synthesis of Allylazo Compounds by Reactions of Aryldiazonium Salts with Allylsilanes

Mayr, Herbert,Grimm, Klaus

, p. 1057 - 1059 (2007/10/02)

Aryldiazonium tetrafluoroborates react with allylsilanes to yield allylazo compounds.If the allylic carbon attached to the azo group carries hydrogen, tautomerization with formation of hydrazones takes place.

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