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5751-83-7 Usage

Chemical Properties

Colourless to light yellow liquid

Uses

Ethyl 5-bromothiophene-2-carboxylate is used as an intermediate in organic syntheses

Check Digit Verification of cas no

The CAS Registry Mumber 5751-83-7 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 5751-83:
(6*5)+(5*7)+(4*5)+(3*1)+(2*8)+(1*3)=107
107 % 10 = 7
So 5751-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrO2S/c1-2-10-7(9)5-3-4-6(8)11-5/h3-4H,2H2,1H3

5751-83-7 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (B22355)  Ethyl 5-bromothiophene-2-carboxylate, 99%   

  • 5751-83-7

  • 1g

  • 495.0CNY

  • Detail
  • Alfa Aesar

  • (B22355)  Ethyl 5-bromothiophene-2-carboxylate, 99%   

  • 5751-83-7

  • 5g

  • 1683.0CNY

  • Detail
  • Alfa Aesar

  • (B22355)  Ethyl 5-bromothiophene-2-carboxylate, 99%   

  • 5751-83-7

  • 25g

  • 3637.0CNY

  • Detail

5751-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-bromothiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-bromothiophen-2-carboxylic acid ethyl ester

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:5751-83-7 SDS

5751-83-7Relevant articles and documents

New iridium-containing conjugated polymers for polymer solar cell applications

Keshtov,Kuklin,Konstantinov,Chen, Fang-Chung,Xie, Zhi-yuan,Sharma, Ganesh D.

, p. 17296 - 17302 (2018)

A series of novel donor-acceptor (D-A) copolymers P1-P5 with iridium-complexed moieties in their side chains have been synthesized on the basis of a new iridium-containing monomer. The results obtained show that P1-P5 have good thermal stability (317-347 °C) for photovoltaic applications. These copolymers absorb visible light in a broad spectral range up to 680 nm. The optical bandgaps of P1-P5 are in the range of 1.96-2.08 eV, respectively. The HOMO and LUMO energy levels of the polymers P1-P5 estimated from cyclic voltammetry measurements indicate that these copolymers are suitable as electron donors along with PC71BM as an electron acceptor for bulk heterojunction polymer solar cells. BHJ polymer solar cells were developed based on blend compositions (P1-P5):PC71BM. The values of Jsc, Voc, and FF are in the range of 0.95-4.44 mA cm?2, 0.67-0.69 V and 34.6-56.8%, and the power conversion efficiencies (PCE) are in the range of 0.22-1.74%, respectively, the highest value of 1.74% being for P3. Increase of the photovoltaic parameters was achieved with increasing iridium complex percentage in the polymers due to involvement of triplet effects. The improvement in the efficiency of the triplet-forming polymers P2 and P3 in comparison with P1 appears to be due to the formation of triplet excitons in comparison with singlet excitons in the polymer P1 which does not contain heavy metals. With further increase in the content of iridium complex fragments in the polymers, for example, up to 3 mol% for polymer P4, the efficiency falls to 1.23% and further decreased to 0.22% for P5.

Design, synthesis, biological evaluation and in vivo testing of dual phosphodiesterase 5 (PDE5) and histone deacetylase 6 (HDAC6)-selective inhibitors for the treatment of Alzheimer's disease

Rabal, Obdulia,Sánchez-Arias, Juan A.,Cuadrado-Tejedor, Mar,de Miguel, Irene,Pérez-González, Marta,García-Barroso, Carolina,Ugarte, Ana,Estella-Hermoso de Mendoza, Ander,Sáez, Elena,Espelosin, Maria,Ursua, Susana,Haizhong, Tan,Wei, Wu,Musheng, Xu,Garcia-Osta, Ana,Oyarzabal, Julen

supporting information, p. 506 - 524 (2018/03/21)

We have identified chemical probes that act as dual phosphodiesterase 5 (PDE5) and histone deacetylase 6 (HDAC6)-selective inhibitors (>1 log unit difference versus class I HDACs) to decipher the contribution of HDAC isoforms to the positive impact of dua

Direct conversion of aromatic ketones to arenecarboxylic esters via carbon-carbon bond-cleavage reactions

Yin, Guodong,Gao, Meng,Wang, Zihua,Wu, Yandong,Wu, Anxin

experimental part, p. 369 - 372 (2009/04/07)

Aromatic methyl ketones, ss-keto esters, and trifluoromethyl-l,3- diketones can be directly converted to arene-carboxylic esters via carbon-carbon bond cleavage of pyridinium iodide intermediates in the presence of copper(II) oxide, iodine, pyridine, and potassium carbonate in alcoholic media. The advantages of the present method in terms of good yields, mild reaction conditions, and inexpensive reagents should make this protocol a valuable alternative to the existing methods.

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