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1H-Pyrazole-3,5-diamine, 1-[2-oxo-1-(phenylhydrazono)propyl]-4-(phenylazo)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93585-26-3

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93585-26-3 Usage

Explanation

The compound consists of 19 carbon atoms, 18 hydrogen atoms, 8 nitrogen atoms, and 1 oxygen atom.
2. Complex organic molecule

Explanation

The compound has a complex structure with multiple functional groups attached to it.
3. Contains a pyrazole ring

Explanation

A pyrazole ring is a five-membered heterocyclic ring with two nitrogen atoms and one oxygen atom.
4. Contains a phenyl group

Explanation

A phenyl group is a six-membered carbon ring with alternating single and double bonds, derived from benzene.
5. Contains an azo group

Explanation

An azo group is a diatomic nitrogen-nitrogen bond (-N=N-) with a linear structure, often used as a functional group in organic compounds.
6. Potential applications in organic synthesis, drug development, and material science

Explanation

The unique structure and properties of the compound make it a promising candidate for various applications, but further research and development are needed to determine its precise uses.
7. Potentially hazardous chemical

Explanation

Due to its complex structure and the presence of reactive functional groups, 1H-Pyrazole-3,5-diamine, 1-[2-oxo-1-(phenylhydrazono)propyl]-4-(phenylazo)- may pose risks to human health and the environment, and should be handled with care and proper safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 93585-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,8 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93585-26:
(7*9)+(6*3)+(5*5)+(4*8)+(3*5)+(2*2)+(1*6)=163
163 % 10 = 3
So 93585-26-3 is a valid CAS Registry Number.

93585-26-3SDS

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 3,5-diamino-4-phenylazo-1-<α-phenylhydrazono-α-(acetyl)methyl>pyrazole

1.2 Other means of identification

Product number -
Other names 1-(3,5-Diamino-4-phenylazo-pyrazol-1-yl)-1-(phenyl-hydrazono)-propan-2-one

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:93585-26-3 SDS

93585-26-3Downstream Products

93585-26-3Relevant academic research and scientific papers

Reaction of Hydrazidoyl Chlorides with Heterocyclic Amines and Mercaptans

Ibrahim, M. K. A.,El-Gharib, M. S.,Farag, A. M.,Elghandour, A. H. H.

, p. 836 - 839 (2007/10/02)

The hydrazidoyl chlorides (1) undergo alkylation with 5-amino-1,3-diphenylpyrazole and 3,5-diamino-4-arylazopyrazoles in ethanol/triethylamine to give the pyrazole derivatives 10 and 11 respectively.They also react with thiosalicylic acid, thioglycolic ac

Studies on 3,5-Diaminopyrazole Derivatives

Abed, Nosrat Mustafa,Hafez, Ebtisam Abdel Aziz,Ibrahim, Nadia Sobhy,Mustafa, Mohamed Elsaid

, p. 223 - 228 (2007/10/02)

The behaviour of 3,5-diamino-4-phenylazopyrazole toward a variety of reagents is reported.Several new 3,5-diaminopyrazole derivatives as well as amino derivatives of fused pyrazoles have been prepared.Keywords: Heterocyclic compounds; Fused pyrazoles

Synthesis of Several New Pyrazolotriazoles, Imidazo-pyrazoles, and Pyrazolopyrazines. Reaction of Nitrilimines with Amino- and Oxo-substituted Azoles. II

Elgemeie, G. E. H.,Elfahham, H. A.,Ghozlan, S. A. S.,Elnagdi, M. H.

, p. 1650 - 1652 (2007/10/02)

The reactivity of amino and hydroxy azoles toward nitrilimines and hydrazonoyl halides was investigated.Several novel rotes for synthesis of derivatives of known heterocyclic systems are reported.

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