5650-51-1

Basic information

• Product Name: AKOS BB-9698
• Synonyms: AKOS BB-9698;5,6-DIHYDRO-CYCLOPENTA[B]THIOPHEN-4-ONE;5,6-dihydro-4H-cyclopenta[b]thiophen-4-one;4H-Cyclopenta[b]thiophen-4-one, 5,6-dihydro-
• CAS NO: 5650-51-1
• Molecular Formula: C₇H₆OS
• Molecular Weight: 138.19
• Mol File: 5650-51-1.mol
• Article Data: 9

Chemical Properties

• Melting Point: 115-117℃
• Boiling Point: 240℃
• Flash Point: 99℃
• Appearance: /
• Density: 1.322
• Vapor Pressure: 0.0398mmHg at 25°C
• Refractive Index: 1.624
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: AKOS BB-9698(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS BB-9698(5650-51-1)
• EPA Substance Registry System: AKOS BB-9698(5650-51-1)

Safety Data

• Hazardous Substances Data: 5650-51-1(Hazardous Substances Data)

Usage

General Description

AKOS BB-9698 is a chemical compound with the molecular formula C10H13N3O3. It is also known by its chemical name 1-(2-Furyl)-2, 4-dimethyl-1H-imidazole-5-carboxylic acid. AKOS BB-9698 is commonly used in pharmaceutical research, as it possesses potential pharmacological properties. Its unique molecular structure and functional groups make it a valuable candidate for drug development and medicinal chemistry studies. AKOS BB-9698 shows promise as a potential therapeutic agent and may be useful in the treatment of various diseases and conditions. Further research and exploration of its chemical properties and biological activities are ongoing to fully understand its potential applications.

InChI:InChI=1/C7H6OS/c8-6-1-2-7-5(6)3-4-9-7/h3-4H,1-2H2

Upstream product

• 188290-36-0 thiophene 
• 2680-03-7 N,N-Dimethylacrylamide 
• 5928-51-8 3-(2-thienyl)propanoic acid 
• 16862-05-8 methyl 3-(2-thienyl)propanoate 
• 15690-25-2 3-(2-thienyl)acrylic acid 
• 498-62-4 3-thiophene carboxaldehyde 
• 849769-14-8 1-(thiophen-3-yl)-3-(trimethylsilyl)prop-2-yn-1-ol 

Downstream Products

• 954238-22-3 5,6-dihydro-4H-cyclopenta[b]thiophen-4-ol 
• 1469857-69-9 3-(4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalen-6-yl)phenylamine hydrochloride 
• 1469857-13-3 4-(4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalen-6-yl)phenylamine hydrochloride 
• 1469858-00-1 6-[4-(4-methylpiperazin-1-yl)phenyl]-2-pyridin-3-yl-4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalene hydrochloride 
• 1469857-99-5 5-{6-[4-(4-methylpiperazin-1-yl)phenyl]-4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalen-2-yl}pyridin-2-ylamine hydrochloride 
• 1469857-98-4 5-[6-(4-morpholin-4-ylphenyl)-4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalen-2-yl]pyridin-2-ylamine hydrochloride 
• 1469858-09-0 5-(4-bromobenzoyl)-5,6-dihydrocyclopenta[b]thiophen-4-one 
• 1469857-46-2 (4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalen-6-yl)(4-trifluoromethylphenyl)amine 
• 1469857-52-0 6-(2-fluorophenyl)-4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalene 
• 1469858-30-7 5-(2-fluorobenzoyl)-5,6-dihydrocyclopenta[b]thiophen-4-one 
• 1469857-16-6 6-(4-nitrophenyl)-4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalene 
• 1469858-14-7 5-(4-nitrobenzoyl)-5,6-dihydrocyclopenta[b]thiophen-4-one 
• 1469858-15-8 5-benzoyl-5,6-dihydrocyclopenta[b]thiophen-4-one 
• 1469857-20-2 4'-(4,7-dihydro-1-thia-4,5-diazacyclopenta[a]pentalen-6-yl)-3-methoxybiphenyl-4-ol 

Relevant articles and documents

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Rh(I)-catalyzed cyclization of 1-arylprop-2-yn-1-ol derivatives utilizing rhodium 1,4-migration

A highly useful method for the construction of cyclopentanone derivatives fused with aromatic ring based on hydrorhodation-1,4-rhodium migration sequence is achieved. Treatment of 1-aryl-prop-2-yn-1-ols, which are easily accessible via an addition of acetylides to the corresponding aryl aldehydes, with a catalytic amount of [Rh(cod)2]2(BF4) and P(p-tolyl)3 in the presence of a base gives cyclopentanone derivatives in moderate to good yield. Copyright