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4,5-DIBROMO-1H-PYRROLE-2-CARBOHYDRAZIDE is a chemical compound characterized by the molecular formula C5H5Br2N3O. It is a hydrazide derivative of pyrrole, featuring two bromine atoms attached to the pyrrole ring and a carbohydrazide functional group. 4,5-DIBROMO-1H-PYRROLE-2-CARBOHYDRAZIDE is recognized for its versatile reactivity, allowing it to engage in various organic synthesis reactions, and is valued for its potential applications across different fields due to its unique structural properties.

50371-65-8

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50371-65-8 Usage

Uses

Used in Organic Synthesis:
4,5-DIBROMO-1H-PYRROLE-2-CARBOHYDRAZIDE is used as a reagent in organic synthesis for its ability to react with a range of organic compounds, facilitating the formation of new chemical bonds. Its reactivity is particularly useful in the preparation of heterocyclic compounds, which are important in various chemical and pharmaceutical applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4,5-DIBROMO-1H-PYRROLE-2-CARBOHYDRAZIDE is utilized as a building block for the development of new drugs. Its unique structure and reactivity contribute to the creation of novel molecular entities with potential therapeutic properties.
Used in Agrochemical Industry:
4,5-DIBROMO-1H-PYRROLE-2-CARBOHYDRAZIDE is employed as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its role in these applications is to provide a foundation for the development of compounds that can effectively control pests and weeds in agricultural settings.
Used in Materials Science:
In the field of materials science, 4,5-DIBROMO-1H-PYRROLE-2-CARBOHYDRAZIDE is used as a component in the development of new materials with specific properties. Its structural characteristics and reactivity can contribute to the creation of materials with tailored characteristics for various applications, such as in electronics or advanced materials research.

Check Digit Verification of cas no

The CAS Registry Mumber 50371-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50371-65:
(7*5)+(6*0)+(5*3)+(4*7)+(3*1)+(2*6)+(1*5)=98
98 % 10 = 8
So 50371-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H5Br2N3O/c6-2-1-3(5(11)10-8)9-4(2)7/h1,9H,8H2,(H,10,11)

50371-65-8SDS

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 4,5-Dibromo-1H-pyrrole-2-carbohydrazide

1.2 Other means of identification

Product number -
Other names dibromopyrrolecarbohydrazide

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:50371-65-8 SDS

50371-65-8Relevant academic research and scientific papers

Synthesis and evaluation of novel 1,3,4-oxadiazole derivatives of marine bromopyrrole alkaloids as antimicrobial agent

Rane, Rajesh A.,Gutte, Shweta D.,Sahu, Niteshkumar U.

, p. 6429 - 6432 (2012/10/30)

In an attempt to identify new potential lead as antimicrobial agent, twenty hybrids of marine bromopyrrole alkaloids with 1,3,4-oxadiazole were designed based on molecular hybridization technique and synthesized. Synthesized molecules were evaluated for t

4,5-Dihalopyrrole-2-carboxamides

-

, (2008/06/13)

4,5-Dihalopyrrole-2-carboxamide derivatives, prepared by reaction of a corresponding 4,5-dihalopyrrole-2-carboxylic acid halide or a corresponding 4,5-dihalopyrrol-2-yl trihalomethyl ketone with an appropriate amine, useful as antibacterial and herbicidal

Herbicidal pyrrole-2-carboxamides

-

, (2008/06/13)

4,5-Dihalopyrrole-2-carboxamide derivatives, prepared by reaction of a corresponding 4,5-dihalopyrrole-2-carboxylic acid halide or a corresponding 4,5-dihalopyrrol-2-yl trihalomethyl ketone with an appropriate amine, have antibacterial and herbicidal acti

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