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Ethyl 5-bromo-4-nitrothiophene-2-carboxylate is a chemical compound characterized by its molecular formula C8H6BrNO4S and a molecular weight of 274.10 g/mol. It is a yellow crystalline solid that serves as a key intermediate in the synthesis of various biologically active substances and pharmaceuticals.

2160-52-3

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2160-52-3 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 5-bromo-4-nitrothiophene-2-carboxylate is utilized as a versatile building block for the synthesis of important compounds in the pharmaceutical industry. Its unique structure allows for the creation of biologically active substances and pharmaceuticals, contributing to the development of new drugs and therapies.
Used in Organic Chemistry:
In the field of organic chemistry, ethyl 5-bromo-4-nitrothiophene-2-carboxylate is employed as a reagent in the synthesis of novel molecules with potential medicinal properties. Its chemical properties enable the formation of new compounds that can be further explored for their therapeutic applications.
Used in Research and Development:
Ethyl 5-bromo-4-nitrothiophene-2-carboxylate is also used in research and development applications for the creation of new drug candidates and molecular probes. Its presence in various chemical reactions aids in the discovery of innovative compounds with potential applications in medicine and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 2160-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2160-52:
(6*2)+(5*1)+(4*6)+(3*0)+(2*5)+(1*2)=53
53 % 10 = 3
So 2160-52-3 is a valid CAS Registry Number.

2160-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-bromo-4-nitrothiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Brom-3-nitro-thiophen-5-carbonsaeure-aethylester

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:2160-52-3 SDS

2160-52-3Downstream Products

2160-52-3Relevant academic research and scientific papers

Discovery of thiophene-2-carboxylic acids as potent inhibitors of HCV NS5B polymerase and HCV subgenomic RNA replication. Part 1: Sulfonamides

Chan, Laval,Das, Sanjoy K.,Reddy, T. Jagadeeswar,Poisson, Carl,Proulx, Melanie,Pereira, Oswy,Courchesne, Marc,Roy, Caroline,Wang, Wuyi,Siddiqui, Arshad,Yannopoulos, Constantin G.,Nguyen-Ba, Nghe,Labrecque, Denis,Bethell, Richard,Hamel, Martine,Courtemanche-Asselin, Philippe,L'Heureux, Lucille,David, Maud,Nicolas, Olivier,Brunette, Stephanie,Bilimoria, Darius,Bedard, Jean

, p. 793 - 796 (2004)

The discovery of a novel class of HCV NS5B polymerase inhibitors, 3-arylsulfonylamino-5-phenyl-thiophene-2-carboxylic acids is described. SAR studies have yielded several potent inhibitors of HCV polymerase as well as of HCV subgenomic RNA replication in

DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS

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Paragraph 0298; 0299, (2014/01/07)

Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols according to formula (I) are useful as inhibitors of the phosphodiesterase 4 (PDE4) enzyme.

DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS

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Page/Page column 70, (2014/01/08)

The invention relates to inhibitors of the phosphodiesterase 4 (PDE4) enzyme. More particularly, the invention relates to compounds that are derivatives of 1 -phenyl-2-pyridinyl alkyl alcohols, methods of preparing such compounds, compositions containing them and therapeutic use thereof.

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