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methyl 4-sulfamoylthiophene-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59337-78-9

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59337-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59337-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,3 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59337-78:
(7*5)+(6*9)+(5*3)+(4*3)+(3*7)+(2*7)+(1*8)=159
159 % 10 = 9
So 59337-78-9 is a valid CAS Registry Number.

59337-78-9SDS

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 methyl 4-sulfamoylthiophene-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 4-(aminosulfonyl)-3-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:59337-78-9 SDS

59337-78-9Relevant academic research and scientific papers

2-AMINO-N-(AMINO-OXO-ARYL-LAMBDA6-SULFANYLIDENE)ACETAMIDE COMPOUNDS AND THEIR THERAPEUTIC USE

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Page/Page column 207; 231, (2021/06/26)

The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain 2-amino-N-(amino-oxo-aryl-λ6- sulfanylidene)acetamide compounds (referred to herein as ANASIA compounds) that, inter alia, inhibit (e.g., selectively inhibit) bacterial aminoacyl-tRNA synthetase (aaRS) (e.g., bacterial leucyl-tRNA synthetase, LeuRS). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit (e.g., selectively inhibit) bacterial aminoacyl-tRNA synthetase; to treat disorders that are ameliorated by the inhibition (e.g., selective inhibition) of bacterial aminoacyl-tRNA synthetase; to treat bacterial infections; etc.

SEMICONDUCTING POLYMERS AND TERNARY BLENDS THEREOF

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Paragraph 0084; 0094, (2016/08/17)

Semiconducting photovoltaic polymers and compositions are disclosed. The polymers and compositions exhibit increased power conversion efficiency in solar cells and other applications.

AMIDINO COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS

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Page/Page column 27-28, (2010/02/12)

The present invention is directed to compounds that are inhibitors of cysteine proteases, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.

Synthesis and anti-inflammatory evaluation of new sulfamoylheterocarboxylic derivatives

Diaz, Juan A.,Morante, M. Esther,Vega, Salvador,Darias, Victoriano,Abdala, Susana,Delgado, Laura,De Las Heras, Beatriz,Villar, Angel,Vivas, Jose Maria

, p. 229 - 238 (2007/10/03)

A series of new sulfamoylthiophene and sulfamoylpyrazole carboxylic acid derivatives was synthesized. Some of these compounds show interesting analgesic properties and significant nonsteroidal anti-inflammatory activities in several models of inflammation.

Aromatization of Dihydrothiophenes. Thiophenesaccharin: A Sweet Surprise

Rossy, Phillip A.,Hoffmann, Werner,Mueller, Norbert

, p. 617 - 620 (2007/10/02)

Sulfuryl chloride has been shown to be highly effective in the dehydrogenation of 3,4-disubstituted-2,5-dihydrothiophenes and 2,3-disubstituted-4,5-dihydrothiophenes, in which the 3,4 and 2,3 substitutents are part of a β-keto carbonyl functionality or it

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