Weight | 134.203 g/mol |
---|---|
Formula | C8H6S |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
Benzo[b]thiophene (95-15-8)
benzothiophene · thianaphthene · benzo(b)thiophene
Score:
#1917 in Physics
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#4724 in Biology
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#6005 in Chemistry
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- Highly Soluble [1]Benzothieno[3,2-b]benzothiophene (BTBT) Derivatives for High-Performance, Solution-Processed Organic Field-Effect Transistors (Journal of the American Chemical Society, 2007)
- Antiestrogens. 2. Structure-activity studies in a series of 3-aroyl-2-arylbenzo[b]thiophene derivatives leading to [6-hydroxy-2-(4-hydroxyphenyl)benzo[b]thien-3-yl] [4-[2-(1-piperidinyl)ethoxy]-phenyl]methanone hydrochloride (LY156758), a remarkably effective estrogen antagonist with only minimal intrinsic estrogenicity. (Journal of Medicinal Chemistry, 1984)
- 2,7-Diphenyl[1]benzothieno[3,2-b]benzothiophene, A New Organic Semiconductor for Air-Stable Organic Field-Effect Transistors with Mobilities up to 2.0 cm2 V-1 s-1 (Journal of the American Chemical Society, 2006)
- Antagonism of estrogen action with a new benzothiophene derived antiestrogen (Life Sciences, 1983)
- Novel Benzofuran and Benzothiophene Biphenyls as Inhibitors of Protein Tyrosine Phosphatase 1B with Antihyperglycemic Properties (Journal of Medicinal Chemistry, 2000)
- N-((1S)-1-{[4-((2S)-2-{[(2,4-Dichlorophenyl)sulfonyl]amino}-3-hydroxypropanoyl)-1-piperazinyl]carbonyl}-3-methylbutyl)-1-benzothiophene-2-carboxamide (GSK1016790A), a Novel and Potent Transient Receptor Potential Vanilloid 4 Channel Agonist Induces Urinary Bladder Contraction and Hyperactivity: Part I (Journal of Pharmacology and Experimental Therapeutics, 2008)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - benzothiophene
- thianaphthene
- benzo(b)thiophene
-
SMILESC1=CC=C2C(=C1)C=CS2
-
InChIKeyFCEHBMOGCRZNNI-UHFFFAOYSA-N
- Pubchem - Benzo[b]thiophene
- Wikipedia - thianaphthene
Benzothiophene is an aromatic organic compound with a molecular formula C8H6S and an odor similar to naphthalene (mothballs). It occurs naturally as a constituent of petroleum-related deposits such as lignite tar. Benzothiophene has no household use.
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5-Methylbenzo[b]thiophene
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benzo[b]thiophene-5-carbaldehyde
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benzo[b]thiophen-4-ol
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Thioxanthen-9-one
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(1-benzothien-2-ylmethyl)amine hydrochloride
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benzo[b]thiophen-2-ylmethanamine
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dibenzo[b,d]thien-2-ylboronic acid
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dibenzo[b,d]thien-2-ylboronic acid hydrate
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Benzo[b]thiophene-2-carboxaldehyde
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benzo[b]thiophene-2-carbonitrile
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(1-benzothien-2-ylmethyl)methylamine hydrochloride
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Thieno[3,2-c]pyridine
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dibenzo[b,d]thiophene-4-carbaldehyde
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5-Chloro-3-methylbenzo[b]thiophene
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Benzo[b]thiophene-2-carboxylic acid
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benzo[b]thiophene-4-carboxylic acid
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1505-62-0
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benzo[b]thiophene-2-carbohydrazide
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3-(3-Benzothienyl)-D-alanine
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23046-03-9
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6-(1,1-dimethylpropyl)-1-benzothiophene-3-carboxylic acid
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