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Propanoic acid, 2-[(2,4-dinitrophenyl)hydrazono]-, methyl ester is a chemical compound with the molecular formula C10H11N5O5. It is a derivative of propanoic acid, where the carboxylic acid group is esterified with methanol, and the remaining carboxylic acid group forms a hydrazone with 2,4-dinitrophenylhydrazine. Propanoic acid, 2-[(2,4-dinitrophenyl)hydrazono]-, methyl ester is characterized by its yellow crystalline appearance and is soluble in common organic solvents such as ethanol and acetone. It is primarily used as a reagent in chemical analysis and synthesis, particularly in the detection and quantification of aldehydes and ketones due to its ability to form colored complexes with these compounds. The compound's structure and properties make it a valuable tool in various analytical techniques, contributing to its importance in the field of chemistry.

3618-76-6

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3618-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3618-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3618-76:
(6*3)+(5*6)+(4*1)+(3*8)+(2*7)+(1*6)=96
96 % 10 = 6
So 3618-76-6 is a valid CAS Registry Number.

3618-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Brenztraubensaeure-methylester-(2,4-dinitro-phenylhydrazon)

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:3618-76-6 SDS

3618-76-6Relevant academic research and scientific papers

Reactions of hydroxyl-containing compounds with tert-butyl hydroperoxide in the presence of chromium tetra-tert-butoxide

Stepovik,Zaburdaeva,Fukin,Karaghiosoff

, p. 2547 - 2559 (2015/12/30)

Primary and secondary aliphatic, alkylaromatic, cyclic, and organoelement alcohols are efficiently oxidized by tert-butyl hydroperoxide in the presence of both equimolar and catalytic quantities of chromium tetra-tert-butoxide (C6H6, 20°C). α-Diols containing tertiary hydroxyl groups interact with this system via oxidative splitting of the carbon scaffold. The oxidation includes the stages of formation and decomposition of chromium-containing peroxy compounds. Further transformations of the carbonyl compounds depend on the structure of radicals in the molecules.

Specific features of the reaction of vanadyl acetylacetonate with tert-butyl hydroperoxide

Stepovik,Gulenova

experimental part, p. 1663 - 1670 (2011/05/14)

Reaction of vanadyl acetylacetonate with tert-butyl hydroperoxide (benzene, 20°C) at any molar ratio leads to the elimination of ligand and its oxidation mainly to CO2 and acetic acid. At the (acac)2VO: t-BuOOH ratio above 1:10 liberation of oxygen partially in the singlet state takes place.

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