CAS 1468-84-4
:5,6-Dihydrobenzo[b]thiophen-7(4H)-one
Description:
5,6-Dihydrobenzo[b]thiophen-7(4H)-one, with the CAS number 1468-84-4, is an organic compound characterized by its fused ring structure that includes both a benzene and a thiophene moiety. This compound features a carbonyl group (ketone) at the 7-position of the thiophene ring, contributing to its reactivity and potential applications in organic synthesis. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the thiophene ring imparts unique electronic properties, making it of interest in materials science and medicinal chemistry. Its derivatives may exhibit biological activity, which has led to research into its potential pharmaceutical applications. The compound's stability and reactivity can be influenced by substituents on the aromatic rings, and it may participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic addition. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken.
Formula:C8H8OS
InChI:InChI=1S/C8H8OS/c9-7-3-1-2-6-4-5-10-8(6)7/h4-5H,1-3H2
InChI key:InChIKey=JEJQJCKVMQVOHZ-UHFFFAOYSA-N
SMILES:O=C1C2=C(CCC1)C=CS2
Synonyms:- 5,6-Dihydrobenzo[b]thiophen-7(4H)-one
- 5,6-dihydro-4H-benzothiophen-7-one
- Benzo[b]thiophen-7(4H)-one, 5,6-dihydro-
- Rarechem Ak Ma K002
- Thiopheno[2′,3′:1,2]cyclohexan-6-one
- 5,6-Dihydro-4H-benzo[b]thiophen-7-one
- 5,6-Dihydro-1-benzothiophene-7(4H)-one
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Found 5 products.
Benzo[b]thiophen-7(4H)-one, 5,6-dihydro-
CAS:Formula:C8H8OSPurity:98%Color and Shape:SolidMolecular weight:152.21354,5,6,7-Tetrahydro-1-benzothiophen-7-one
CAS:4,5,6,7-Tetrahydro-1-benzothiophen-7-onePurity:98%Molecular weight:152.21g/mol5,6-Dihydrobenzo[b]thiophen-7(4H)-one
CAS:Controlled ProductFormula:C8H8OSColor and Shape:NeatMolecular weight:152.215,6-Dihydrobenzo[b]thiophen-7(4H)-one
CAS:<p>5,6-Dihydrobenzo[b]thiophen-7(4H)-one is a sulfur-containing heterocycle that has been shown in studies to have cytotoxic activity. This compound has been found to induce apoptosis (programmed cell death) in cancer cells by binding to the protein kinase B (PKB/Akt), which is involved in the regulation of cell proliferation and survival. 5,6-Dihydrobenzo[b]thiophen-7(4H)-one also binds to DNA, preventing transcription and translation of proteins. The cytotoxic effects of this compound make it useful for treatment of ophthalmic conditions such as cataracts and glaucoma. This compound is being studied for use in the treatment of ovarian cancer and other types of cancer. It was recently shown that 5,6-dihydrobenzo[b]thiophen-7(4H)-one</p>Formula:C8H8OSPurity:Min. 95%Molecular weight:152.21 g/mol




