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13191-40-7

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13191-40-7 Usage

General Description

3-(2,5-DIBROMOTHIEN-3-YL)PROPANOIC ACID is a chemical compound with the molecular formula C9H9Br2O2S. It is a synthetic organic compound and a derivative of thiophene, containing both bromine and carboxylic acid functional groups. 3-(2,5-DIBROMOTHIEN-3-YL)PROPANOIC ACID is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also used in the production of specialty polymers and materials. Additionally, it has potential applications in the field of organic electronics, as it can be incorporated into the design of organic semiconductors and optoelectronic devices. Due to its unique structure and functional groups, 3-(2,5-DIBROMOTHIEN-3-YL)PROPANOIC ACID has a wide range of uses in the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13191-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,9 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13191-40:
(7*1)+(6*3)+(5*1)+(4*9)+(3*1)+(2*4)+(1*0)=77
77 % 10 = 7
So 13191-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Br2O2S/c8-5-3-4(7(9)12-5)1-2-6(10)11/h3H,1-2H2,(H,10,11)

13191-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,5-dibromothiophen-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2,4-DICHLOROBENZAMIDINE HCL

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:13191-40-7 SDS

13191-40-7Relevant articles and documents

Novel synthesis of thianinhydrin

Hauze, Diane B.,Joullie, Madeleine M.,Ramotowski, Robert,Cantu, Antonio

, p. 4239 - 4246 (1997)

The synthesis of the previously reported thianinhydrin (12) was achieved from 3-methylthiophene via the corresponding 5,6-dihydrocyclopenta[b]thiophen-4,6-dione (10). Conversion of 10 to the tricarbonyl (12) proceeded in good yield using dimethydioxirane oxidation of 5,6-dihydro-5-dimethyl aminomethylenecyclopenta[b]thiophen-4,6-dione (14). The fluorescence intensity of the zinc salt of the product of 12 and glycine was similar to that obtained from the product of ninhydrin and the same amino acid.

SPIRO RING COMPOUND AS HEPATITIS C VIRUS (HCV) INHIBITOR AND USES THEREOF FIELD OF THE INVENTION

-

Page/Page column 210; 211; 212, (2014/06/23)

A compound of formula (I) or a stereoisomer, a geometric isomer. a tautomer, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof is provided, which can be used for treating HCV infection or a HCV disorder. Also a pharmaceutical composition comprising the compound and the use of the compound and the pharmaceutical composition thereof are provided, which can also be used for treating HCV infection or a HCV disorder.

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