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(2Z)-1-(2,4-dinitrophenyl)-2-(1,2,2-trimethylpropylidene)hydrazine is a hydrazine derivative featuring a dinitrophenyl and a trimethylpropylidene moiety. It is a key reagent in organic synthesis and medicinal chemistry for the preparation of pharmaceuticals and biologically active compounds. (2Z)-1-(2,4-dinitrophenyl)-2-(1,2,2-trimethylpropylidene)hydrazine is known for its potential antimicrobial, anti-inflammatory, and antitumor activities, and it serves as a reagent in developing selective and specific chemical reactions. Its unique chemical structure and reactivity contribute to its value in chemical research and development.

964-53-4

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964-53-4 Usage

Uses

Used in Pharmaceutical Industry:
(2Z)-1-(2,4-dinitrophenyl)-2-(1,2,2-trimethylpropylidene)hydrazine is used as a key reagent for the synthesis of various pharmaceuticals and biologically active compounds, due to its ability to facilitate the creation of complex organic molecules.
Used in Organic Synthesis:
In the field of organic synthesis, (2Z)-1-(2,4-dinitrophenyl)-2-(1,2,2-trimethylpropylidene)hydrazine is utilized as a reagent for developing selective and specific chemical reactions, contributing to the advancement of chemical processes and methodologies.
Used in Medicinal Chemistry:
(2Z)-1-(2,4-dinitrophenyl)-2-(1,2,2-trimethylpropylidene)hydrazine is employed as a reagent in medicinal chemistry for the preparation of compounds with potential antimicrobial, anti-inflammatory, and antitumor activities, highlighting its role in the discovery and development of new therapeutic agents.
Used in Chemical Research and Development:
(2Z)-1-(2,4-dinitrophenyl)-2-(1,2,2-trimethylpropylidene)hydrazine is used as a valuable tool in chemical research and development, owing to its unique chemical structure and reactivity, which can lead to innovative applications and discoveries in the chemical sciences.

Check Digit Verification of cas no

The CAS Registry Mumber 964-53-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 964-53:
(5*9)+(4*6)+(3*4)+(2*5)+(1*3)=94
94 % 10 = 4
So 964-53-4 is a valid CAS Registry Number.

964-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,3-dimethylbutan-2-ylideneamino)-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names pinacoline 2,4-dinitrophenylhydrazone

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:964-53-4 SDS

964-53-4Downstream Products

964-53-4Relevant academic research and scientific papers

Reactions of regioisomeric fluoroalkyl-containing β-aminovinyl ketones with hydrazines

Pashkevich,Filyakova,Kuznetsova

, p. 2868 - 2870 (2007/10/03)

Fluoroalkyl β-alkyl-β-aminovinyl ketones react with hydrazine hydrate to give the respective pyrazoles, and with phenylhydrazine they form a mixture of pyrazoles and 5-hydroxy-Δ2-pyrazolines. Alkyl(aryl) β-fluoroalkyl-β-aminovinylketones do not react with the hydrazines mentioned above. With 2,4-dinitrophenylhydrazine, both types of fluoroalkyl-containing β-aminovinyl ketones give only hydrazones of the corresponding methyl alkyl(aryl) ketones.

Synthesis and formal [4 + 2] cycloaddition reactions of vinylimido complexes of titanocene

Doxsee, Kenneth M.,Farahi, Judah B.,Hope, H?kon

, p. 8889 - 8898 (2007/10/02)

Sources of the methylidene complex of titanocene, Cp2Ti=CH2, react with nitriles in the presence of donor ligands to afford vinylimido titanocene complexes. The vinylimido complexes react readily with ketones, nitriles, and imines, y

New Methods and Reagents in Organic Synthesis; 73. Trimethylsilyldiazomethane: A Convenient Reagent for the Conversion of Aliphatic Aldehydes to the Homologous Methyl Ketones

Aoyama, Toyohiko,Shioiri, Takayuki

, p. 228 - 229 (2007/10/02)

Trimethylsilyldiazomethane reacts smoothly with aliphatic aldehydes in the presence of magnesium bromide (1.5 eqiv) to give homologous methyl ketones after direct treatment with 10percent hydrochloric acid/methanol (1:1).

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