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5813-89-8

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5813-89-8 Usage

Chemical Properties

white crystalline powder

Uses

2-Thiophenecarboxamide is a small molecule DnaK modulator targeting the β (nucleotide binding) domain for potential use as antibacterial agent.

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 2779, 1951 DOI: 10.1021/ja01150a103

Check Digit Verification of cas no

The CAS Registry Mumber 5813-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5813-89:
(6*5)+(5*8)+(4*1)+(3*3)+(2*8)+(1*9)=108
108 % 10 = 8
So 5813-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H5NOS/c6-5(7)4-2-1-3-8-4/h1-3H,(H2,6,7)

5813-89-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (A15219)  Thiophene-2-carboxamide, 99%   

  • 5813-89-8

  • 5g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (A15219)  Thiophene-2-carboxamide, 99%   

  • 5813-89-8

  • 25g

  • 1443.0CNY

  • Detail
  • Aldrich

  • (164453)  2-Thiophenecarboxamide  99%

  • 5813-89-8

  • 164453-5G

  • 466.83CNY

  • Detail

5813-89-8SDS

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 2-Thiophenecarboxamide

1.2 Other means of identification

Product number -
Other names 2-THIOPHENECARBOXAMIDE

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:5813-89-8 SDS

5813-89-8Relevant articles and documents

Mechanochemical synthesis of half-sandwich iridium/rhodium complexes with 8-hydroxyquinoline derivatives ligands

Jia, Wei-Guo,Li, Xiao-Dong,Zhi, Xue-Ting,Zhong, Rui

, (2022/01/19)

Mechanochemistry provides a rapid, efficient route to half-sandwich iridium and rhodium complexes from [MCp*(μ-Cl)Cl]2 (M = Ir, Rh) and 8-hydroxyquinoline-2-carbaldehyde without the need for Schlenk manipulation, inert gas protection, or dry solvents. Furthermore, post-synthetic modification of the half-sandwich metal complexes has been carried out via a mechanochemical Wittig reaction between half-sandwich metal complex and phosphorus ylide. All complexes were fully characterized by 1H and 13C NMR spectra, infrared spectroscopy, mass spectrometry, and single-crystal X-ray diffraction method. The half-sandwich rhodium complexes exhibited high catalytic activity towards the amide synthesis between aldehyde and hydroxylamine hydrochloride (NH2OH·HCl) with a broad functional group tolerance.

Lead derivatization of ethyl 6-bromo-2-((dimethylamino)methyl)-5-hydroxy-1-phenyl-1H-indole-3-carboxylate and 5-bromo-2-(thiophene-2-carboxamido) benzoic acid as FabG inhibitors targeting ESKAPE pathogens

Varakala, Saiprasad Dasugari,Reshma, Rudraraju Srilakshmi,Schnell, Robert,Dharmarajan, Sriram

, (2021/11/26)

Our previous studies on FabG have identified two compounds 5-bromo-2-(thiophene-2-carboxamido) benzoic acid (A) and ethyl 6-bromo-2-((dimethylamino)methyl)-5-hydroxy-1-phenyl-1H-indole-3-carboxylate(B) as best hits with allosteric mode of inhibition. FabG is an integral part of bacterial fatty acid biosynthetic system FAS II shown to be an essential gene in most ESKAPE Pathogens. The current work is focussed on lead expansion of these two hit molecules which ended up with forty-three analogues (twenty-nine analogues from lead compound A and fourteen compounds from lead compound B). The enzyme inhibition studies revealed that compound 15 (effective against EcFabG, AbFabG, StFabG, MtFabG1) and 19 (inhibiting EcFabG and StFabG) had potency of broad-spectrum inhibition on FabG panel.

Single-pot tandem oxidative/C-H modification amidation process using ultrasmall PdNP-encapsulated porous organosilica nanotubes

Gholipour, Behnam,Liu, Xiao,Rostamnia, Sadegh,Zonouzi, Afsaneh

, p. 4276 - 4287 (2022/02/16)

Herein, we studied a single-pot method with a dual catalysis process towards the conversion of primary aromatic alcohols to amides using ultrasmall PdNPs of controlled uniform size (1.8 nm) inside hybrid mesoporous organosilica nanotubes (MO-NTs). The cat

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