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[4-(3,3-dimethyltriazanyl)phenyl](E)-[hydroxy(4-nitrophenyl)methyl]diazenylmethanone is a complex diazo and azo compound characterized by the presence of a triazanyl group, a phenyl group, and a nitrophenyl group. Its structure is defined by the substituents attached to the azo group, with the dimethyltriazanyl group and the hydroxy(4-nitrophenyl)methyl group being particularly noteworthy. [4-(3,3-dimethyltriazanyl)phenyl](E)-[hydroxy(4-nitrophenyl)methyl]diazenylmethanone holds potential for use in organic synthesis and as a reagent in chemical reactions due to its reactive functional groups, which can participate in reactions like diazotization and azo coupling. However, it is crucial to exercise caution when handling [4-(3,3-dimethyltriazanyl)phenyl]{(E)-[hydroxy(4-nitrophenyl)methyl]diazenyl}methanone, as azo compounds can pose certain hazards.

62591-65-5

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62591-65-5 Usage

Uses

Used in Organic Synthesis:
[4-(3,3-dimethyltriazanyl)phenyl](E)-[hydroxy(4-nitrophenyl)methyl]diazenylmethanone is used as a synthetic building block for creating a variety of complex organic molecules. Its unique combination of functional groups allows for versatile reactivity in chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, dyes, and other specialty chemicals.
Used in Chemical Reactions as a Reagent:
In the chemical industry, [4-(3,3-dimethyltriazanyl)phenyl](E)-[hydroxy(4-nitrophenyl)methyl]diazenylmethanone serves as a reagent that can facilitate specific chemical transformations. Its diazo and azo functional groups are key to its reactivity, enabling it to participate in diazotization and azo coupling reactions, which are important for the production of various chemical products.
Used in Research and Development:
[4-(3,3-dimethyltriazanyl)phenyl](E)-[hydroxy(4-nitrophenyl)methyl]diazenylmethanone is also utilized in research and development settings, where its unique properties can be explored for new applications and to understand its reactivity and potential interactions with other molecules. The study of such compounds contributes to the advancement of chemical knowledge and can lead to the discovery of new materials and processes.
Safety Note:
It is important to handle [4-(3,3-dimethyltriazanyl)phenyl](E)-[hydroxy(4-nitrophenyl)methyl]diazenylmethanone with care, as azo compounds can be potentially hazardous. Special safety measures should be taken during its handling and use to minimize risks associated with its reactivity and potential toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 62591-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,9 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62591-65:
(7*6)+(6*2)+(5*5)+(4*9)+(3*1)+(2*6)+(1*5)=135
135 % 10 = 5
So 62591-65-5 is a valid CAS Registry Number.

62591-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(dimethylamino)hydrazinyl]-N-[hydroxy-(4-nitrophenyl)methyl]iminobenzamide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62591-65-5 SDS

62591-65-5Upstream product

62591-65-5Downstream Products

62591-65-5Relevant academic research and scientific papers

Preparation and antitumor activity of 1 aryl 3,3 dimethyltriazene derivatives

Giraldi,Nisi,Connors,Goddard

, p. 850 - 853 (2007/10/08)

Several 1-aryl-3, 3-dimethyltriazene derivatives have been synthesized and tested for their antitumor activity against the TLX5 lymphoma in mice. These compounds are characterized by the presence of a carbonyl group bound to the benzene nucleus in the para position to the triazene function. Three p-sulfamoyl derivatives have also been included and proved to be inactive. Among the carbonyl derivatives compounds 1 and 20, which can be used as reference, cause ILS of about 50%, respectively, at four and three dose levels. Compound 16, the o-nitrophenylhydrazone of the hydrazide 1, is active at all six dose levels studied. The adduct 19, obtained from the same hydrazide and p-nitrobenzaldehyde, is active at four dose levels, and the ILS value at two optimum doses are significantly greater than those caused by compound 1.

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