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2-BROMO-4-CYANOTHIOPHENE, with the molecular formula C6H3BrNS, is a derivative of thiophene, a heterocyclic compound that features a sulfur atom within its five-membered ring. This chemical compound is recognized for its versatility in chemical reactions, particularly cross-coupling reactions, which make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it serves as a building block in the creation of organic electronic materials, including organic light-emitting diodes (OLEDs) and organic photovoltaic cells. As a colorless to light yellow liquid with a distinctive odor, 2-BROMO-4-CYANOTHIOPHENE is classified as a hazardous material due to its flammability and toxicity.

18792-00-2

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18792-00-2 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-BROMO-4-CYANOTHIOPHENE is used as a chemical intermediate for the synthesis of various pharmaceuticals and agrochemicals, leveraging its reactivity in cross-coupling reactions to form complex molecular structures that possess desired therapeutic or pesticidal properties.
Used in Organic Electronics Industry:
2-BROMO-4-CYANOTHIOPHENE is utilized as a building block in the production of organic electronic materials such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells, contributing to the development of advanced electronic devices with improved performance and energy efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 18792-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,9 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18792-00:
(7*1)+(6*8)+(5*7)+(4*9)+(3*2)+(2*0)+(1*0)=132
132 % 10 = 2
So 18792-00-2 is a valid CAS Registry Number.

18792-00-2SDS

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-Bromothiophene-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-bromo4-thiophenecarbonitrile

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:18792-00-2 SDS

18792-00-2Downstream Products

18792-00-2Relevant academic research and scientific papers

2-AMINO-N-(AMINO-OXO-ARYL-LAMBDA6-SULFANYLIDENE)ACETAMIDE COMPOUNDS AND THEIR THERAPEUTIC USE

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Page/Page column 228-229, (2021/06/26)

The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain 2-amino-N-(amino-oxo-aryl-λ6- sulfanylidene)acetamide compounds (referred to herein as ANASIA compounds) that, inter alia, inhibit (e.g., selectively inhibit) bacterial aminoacyl-tRNA synthetase (aaRS) (e.g., bacterial leucyl-tRNA synthetase, LeuRS). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit (e.g., selectively inhibit) bacterial aminoacyl-tRNA synthetase; to treat disorders that are ameliorated by the inhibition (e.g., selective inhibition) of bacterial aminoacyl-tRNA synthetase; to treat bacterial infections; etc.

Random poly(3-hexylthiophene-co-3-cyanothiophene) copolymers with high open-circuit voltage in organic solar cells

Khlyabich, Petr P.,Rudenko, Andrey E.,Thompson, Barry C.

, p. 1055 - 1058 (2014/03/21)

Four novel random poly(3-hexylthiophene) copolymers containing 5-20% of 3-cyanothiophene are synthesized by Stille polycondensation; and their electrochemical, optical, charge transport, and photovoltaic properties are investigated. All polymers show high efficiencies and high open-circuit voltages (Voc) up to 0.81 V with a PC61BM acceptor in organic solar cells. Copyright

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