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2-Thiophenecarboxylic acid, 5-nitro-, ethyl ester is a yellow crystalline chemical compound that belongs to the class of organic compounds known as nitrobenzenes. It is synthesized by reacting 5-nitro-2-thiophenecarboxylic acid with ethanol in the presence of a strong acid catalyst, resulting in a versatile reagent with functional groups that make it a valuable building block in organic chemistry.

5751-84-8

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5751-84-8 Usage

Uses

Used in Pharmaceutical Industry:
2-Thiophenecarboxylic acid, 5-nitro-, ethyl ester is used as a precursor in the synthesis of various pharmaceuticals. Its functional groups and versatile reactivity allow for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Thiophenecarboxylic acid, 5-nitro-, ethyl ester is utilized as a starting material for the production of various agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Organic Chemistry Research:
As an important building block in organic chemistry, 2-Thiophenecarboxylic acid, 5-nitro-, ethyl ester is used in research for the development of new materials and substances, further expanding its applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5751-84-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5751-84:
(6*5)+(5*7)+(4*5)+(3*1)+(2*8)+(1*4)=108
108 % 10 = 8
So 5751-84-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO4S/c1-2-12-7(9)5-3-4-6(13-5)8(10)11/h3-4H,2H2,1H3

5751-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-nitrothiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 5-nitro-2-thiophenecarboxylate

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:5751-84-8 SDS

5751-84-8Relevant academic research and scientific papers

Raltitrexed pharmaceutical composition and preparation method thereof

-

, (2018/04/02)

The invention relates to a raltitrexed pharmaceutical composition which is high in safety and a preparation method thereof. The raltitrexed pharmaceutical composition comprises raltitrexed and thiophene related substances, wherein the content of the thiophene related substances is not higher than 0.3%. The raltitrexed pharmaceutical composition is good in safety, effectiveness and stability and can relieve the blood toxicity of the raltitrexed to a certain degree.

Design, synthesis, and biological evaluation of 2-(phenoxyaryl)-3-urea derivatives as novel P2Y1 receptor antagonists

Peng, Jingjing,Zhao, Lifen,Wang, Lanlan,Chen, Hui,Qiu, Yunguang,Wang, Jiang,Yang, Huaiyu,Liu, Jun,Liu, Hong

, p. 302 - 310 (2018/09/18)

A novel series of 2-(phenoxyaryl)-3-urea derivatives were designed, synthesized, and biologically evaluated for their anti-thrombotic activity. Most of compounds exhibited good inhibition against P2Y1 receptor. Among them, three compounds 11, 12, and 13 demonstrated good P2Y1 receptor antagonistic potency in vitro (IC50 = 0.62 μM, 0.82 μM, and 0.21 μM, respectively). In antiplatelet aggregation study, four compounds 2, 3, 9, and 13 showed good antiplatelet activity. The possible binding modes of compounds with P2Y1 receptor were also explored by molecular docking simulation. The docking studies demonstrated that compound 13 interacted well with Phe119 through hydrophobic interaction and modestly improved the P2Y1 receptor antagonistic activity, making it justifiable for further investigation.

Improved modular synthesis of thieno[3,2-b]pyrroles and thieno[2,3-b]pyrroles

Malancona, Savina,Hernando, Josè I. Martin,Attenni, Barbara,Ontoria, Jesus M.,Narjes, Frank

supporting information; experimental part, p. 1625 - 1628 (2009/06/18)

A convenient modular synthesis for the construction of densely functionalized thieno[3,2-b]pyrroles, allosteric inhibitors of the Hepatitis C virus NS5B polymerase, is described. The route allows the introduction of substituents in positions 4, 5, and 6 o

THIENOPYRROLES AS ANTIVIRAL AGENTS

-

Page/Page column 50, (2008/06/13)

The present invention relates to thienopyrrole compounds of formula (I); wherein A, B, Y, Ar, n, Z and X1 are as defined herein, and pharmaceutically acceptable salts thereof, useful in the prevention and treatment of hepatitis C infections.

Novel acyl hydrazino thiophene derivatives, process for preparing them, their use as medicinal products, pharmaceutical compositions and novel use

-

Page/Page column 20, (2010/02/12)

The invention concerns novel compounds of formula (I), process for making, pharmaceutical compositions and methods of treating diseases associated with abnormal physiological behavior in the secretion and/or the activity of cysteine proteases especially c

Hypolipidemic and antiatherosclerotic novel (monosubstituted-amino)heteroaryl carboxylic acids and analogs

-

, (2008/06/13)

This disclosure described novel (monosubstituted-amino)heteroaryl carboxylic acids and analogs which are useful as hypolipidemic and antiatherosclerotic agents.

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