2-Chlorothiophene

Name: 2-Chlorothiophene | 96-43-5
Brand: US-CATO
SKU: S57C4X-109073_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57C4X-109073_10_MG

Vendor: US-CATO

Product Information

Product Name

2-Chlorothiophene

Brand Name

US-CATO

Product Number

C4X-109073

CAS

96-43-5

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

7299

IUPAC Name

2-chlorothiophene

InChI Key

GSFNQBFZFXUTBN-UHFFFAOYSA-N

SMILES

C1=CSC(=C1)Cl

References

New Cross-Conjugated Isoquinolines from 4H-Thieno[3,2-b]pyrroles

Publication Name: Russian Journal of General Chemistry

Publication Date: 2025-05

DOI: 10.1134/s1070363225601395

Visible light-mediated 1,3-acylative chlorination of cyclopropanes employing benzoyl chloride as bifunctional reagents in NHC catalysis

Publication Name: Science China Chemistry

Publication Date: 2025-03-10

DOI: 10.1007/s11426-024-2525-0

Design and synthesis of benzo[d][d] imidazo[2,1-b]thiazol-8(5H)-ones as potent anti-infective agents

Publication Name: Medicinal Chemistry Research

Publication Date: 2024-05-28

DOI: 10.1007/s00044-024-03240-0

De novo development of small cyclic peptides that are orally bioavailable

Publication Name: Nature Chemical Biology

Publication Date: 2023-12-28

DOI: 10.1038/s41589-023-01496-y

The electronic structure of 2(5H)-thiophenone investigated by vacuum ultraviolet synchrotron radiation and theoretical calculations

Publication Name: The European Physical Journal D

Publication Date: 2023-11

DOI: 10.1140/epjd/s10053-023-00771-w

2-Chlorothiophene

Product Information

General Information

References

New Cross-Conjugated Isoquinolines from 4H-Thieno[3,2-b]pyrroles

Visible light-mediated 1,3-acylative chlorination of cyclopropanes employing benzoyl chloride as bifunctional reagents in NHC catalysis

Design and synthesis of benzo[d][d] imidazo[2,1-b]thiazol-8(5H)-ones as potent anti-infective agents

De novo development of small cyclic peptides that are orally bioavailable

The electronic structure of 2(5H)-thiophenone investigated by vacuum ultraviolet synchrotron radiation and theoretical calculations