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5-Bromo-4-nitrothiophene-2-carbaldehyde is a chemical compound characterized by the molecular formula C6H3BrN2O3S. It is a yellow solid with a molecular weight of 240.06 g/mol. 5-BroMo-4-nitrothiophene-2-carbaldehyde is distinguished by the presence of a bromine atom, a nitro group, and a thiophene ring, which collectively contribute to its versatile chemical properties. These features make it a valuable intermediate in the synthesis of a wide range of organic compounds, including pharmaceuticals and agrochemicals.

79456-86-3

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79456-86-3 Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-4-nitrothiophene-2-carbaldehyde is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications. The presence of a bromine atom and a nitro group provides opportunities for further chemical modifications, enhancing the compound's reactivity and its potential to be incorporated into complex molecular structures.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Bromo-4-nitrothiophene-2-carbaldehyde serves as an intermediate for the production of pesticides and other crop protection agents. Its chemical properties make it suitable for the creation of compounds that can effectively target pests and diseases, thereby contributing to improved agricultural yields and food security.
Used in Organic Chemistry Research:
5-Bromo-4-nitrothiophene-2-carbaldehyde is also used as a research compound in the field of organic chemistry. Its unique structure and properties make it an interesting subject for studies aimed at understanding reaction mechanisms, exploring new synthetic routes, and discovering novel applications in various chemical processes.
Used in the Synthesis of Other Organic Compounds:
Beyond its applications in pharmaceuticals and agrochemicals, 5-Bromo-4-nitrothiophene-2-carbaldehyde is employed as a building block in the synthesis of other organic compounds. Its versatility allows it to be incorporated into a wide array of molecules, potentially leading to the development of new materials, dyes, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 79456-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79456-86:
(7*7)+(6*9)+(5*4)+(4*5)+(3*6)+(2*8)+(1*6)=183
183 % 10 = 3
So 79456-86-3 is a valid CAS Registry Number.

79456-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-4-nitrothiophene-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Thiophenecarboxaldehyde,5-bromo-4-nitro

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:79456-86-3 SDS

79456-86-3Downstream Products

79456-86-3Relevant academic research and scientific papers

Cerebral antihypoxic activity of new thienyldihydropyridines

Boulouard,Louchahi-Raoui,Heude,Quermonne,Cugnon de Sevricourt,Rault,Robba

, p. 162 - 165 (1995)

New thienyldihydropyridines were synthesized according to Hantzsch's method. The antihypoxic activity of these compounds was compared with that of three reference phenyldihydropyridines by means of the skin conductance reaction (SCR)-hypoxia test.

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