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METHYL 4,5-DIBROMOTHIOPHENE-2-CARBOXYLATE is a chemical compound characterized by its molecular formula C7H5Br2O2S. It is a brominated ester derivative of thiophene, an aromatic ring containing sulfur. METHYL4,5-DIBROMOTHIOPHENE-2-CARBOXYLATE is known for its versatile reactivity and functional groups, making it a valuable asset in the synthesis of organic molecules and pharmaceuticals. Additionally, it finds applications in the production of agrochemicals for pest and disease control in agriculture.

62224-24-2

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62224-24-2 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 4,5-DIBROMOTHIOPHENE-2-CARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, METHYL 4,5-DIBROMOTHIOPHENE-2-CARBOXYLATE is utilized in the production of pesticides and other crop protection agents. Its properties contribute to the effectiveness of these products in controlling pests and diseases, thereby ensuring healthier and more productive crops.
Used in Organic Synthesis:
METHYL 4,5-DIBROMOTHIOPHENE-2-CARBOXYLATE is employed as a versatile building block in organic synthesis. Its functional groups and reactivity enable the creation of a wide range of organic molecules for various applications, including materials science, chemical research, and the development of new compounds with specific properties.
Used in Research and Development:
Due to its potential applications across different industries, METHYL 4,5-DIBROMOTHIOPHENE-2-CARBOXYLATE is a valuable chemical for research and development purposes. It serves as a starting material for exploring new chemical reactions, discovering novel compounds, and advancing the understanding of chemical processes and mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 62224-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,2 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62224-24:
(7*6)+(6*2)+(5*2)+(4*2)+(3*4)+(2*2)+(1*4)=92
92 % 10 = 2
So 62224-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Br2O2S/c1-10-6(9)4-2-3(7)5(8)11-4/h2H,1H3

62224-24-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H32113)  Methyl 4,5-dibromothiophene-2-carboxylate, 97%   

  • 62224-24-2

  • 1g

  • 386.0CNY

  • Detail
  • Alfa Aesar

  • (H32113)  Methyl 4,5-dibromothiophene-2-carboxylate, 97%   

  • 62224-24-2

  • 5g

  • 1287.0CNY

  • Detail

62224-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4,5-dibromothiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 4,5-dibromothiophene-2-carboxylate

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:62224-24-2 SDS

62224-24-2Relevant academic research and scientific papers

THIOPHENE, MANUFACTURING METHOD THEREOF, AND PHARMACEUTICAL APPLICATION OF SAME

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Paragraph 0103; 0104; 0105, (2019/04/25)

The present invention discloses a thiophene used as a uric acid transporter (URAT1) inhibitor and applicantion of the thiophene in preparing a pharmaceutical product for treating a disease related to abnormal uric acid levels, specifically in preparing a pharmaceutical product for treating hyperuricemia and gouty arthritis. The invention specifically relates to a compound as represented by formula (I) or a pharmaceutically acceptable salt thereof.

Thieno[3,2-c]pyrazoles: A novel class of Aurora inhibitors with favorable antitumor activity

Bindi, Simona,Fancelli, Daniele,Alli, Cristina,Berta, Daniela,Bertrand, Jay A.,Cameron, Alexander D.,Cappella, Paolo,Carpinelli, Patrizia,Cervi, Giovanni,Croci, Valter,D'Anello, Matteo,Forte, Barbara,Laura Giorgini,Marsiglio, Aurelio,Moll, Juergen,Pesenti, Enrico,Pittalà, Valeria,Pulici, Maurizio,Riccardi-Sirtori, Federico,Roletto, Fulvia,Soncini, Chiara,Storici, Paola,Varasi, Mario,Volpi, Daniele,Zugnoni, Paola,Vianello, Paola

experimental part, p. 7113 - 7120 (2010/10/21)

A novel series of 3-amino-1H-thieno[3,2-c]pyrazole derivatives demonstrating high potency in inhibiting Aurora kinases was developed. Here we describe the synthesis and a preliminary structure-activity relationship, which led to the discovery of a represe

Heterobicyclic pyrazole derivatives as kinase inhibitors

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Page/Page column 23, (2008/06/13)

Bicyclo-pyrazoles of formula (I) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in

Insights into the mechanism of the site-selective sequential palladium-catalyzed cross-coupling reactions of dibromothiophenes/ dibromothiazoles and arylboronic acids. Synthesis of PPARβ/δ agonists

Pereira, Raquel,Furst, Audrey,Iglesias, Beatriz,Germain, Pierre,Gronemeyer, Hinrich,De Lera, Angel R.

, p. 4514 - 4525 (2008/09/19)

A reactivity study, aided by NMR spectroscopy, allowed a mechanistic rationale to be postulated for the palladium-catalyzed regioselective coupling of arylboronic acid (and arylstannane where feasible) at the position next to the sulfur atom in functional

HETEROBICYCLIC PYRAZOLE DERIVATIVES AS KINASE INHIBITORS

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Page 58, (2010/02/06)

Bicyclo-pyrazoles of formula (I) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in

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