55735-44-9

Basic information

• Product Name: Cyclohexanone, 2-(hydroxymethylene)-, sodium salt
• CAS NO: 55735-44-9
• Molecular Formula: C7H10O2.Na
• Molecular Weight: 148.137
• Mol File: 55735-44-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-(hydroxymethylene)-, sodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-(hydroxymethylene)-, sodium salt(55735-44-9)
• EPA Substance Registry System: Cyclohexanone, 2-(hydroxymethylene)-, sodium salt(55735-44-9)

Safety Data

• Hazardous Substances Data: 55735-44-9(Hazardous Substances Data)

Upstream product

• 107-31-3 Methyl formate 
• 108-94-1 cyclohexanone 
• 109-94-4 formic acid ethyl ester 

Downstream Products

• 64230-01-9 2-formyl-2-chlorocyclohexanone 
• 167260-77-7 2-Chloro-2-(hydroxy-methoxy-methyl)-cyclohexanone 
• 315248-91-0 AG-205/33684025 
• 361198-68-7 3-amino-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide 
• 441718-28-1 3-amino-5,6,7,8-tetrahydro-thieno[2,3-b]quinoline-2-carboxylic acid p-tolylamide 
• 340813-02-7 3-amino-N-(4'-methoxyphenyl)-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide 
• 780757-83-7 2-phenyl-7,8,9,10-tetrahydropyrimido[4',5':4,5]thieno[2,3-b]quinoline-4(3H)-one 
• 780757-84-8 4-chloro-2-phenyl-7,8,9,10-tetrahydropyrimido[4',5':4,5]thieno[2,3-b]quinoline 
• 780757-85-9 4-mercapto-2-phenyl-7,8,9,10-tetrahydropyrimido[4',5':4,5]thieno[2,3-b]quinoline 
• 780757-63-3 N'-benzylidene-3-amino-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carbohydrazone 
• 310456-40-7 2-(2-oxo-2-phenyl-ethylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile 

Relevant articles and documents

A Method for the Preparation of β-Amino-α,β-unsaturated Carbonyl Compounds: Study of Solvent Effect and Mechanism

An efficient method for the preparation of β-amino-α,β-unsaturated carbonyl compounds is demonstrated. Bench-stable sodium 3-oxo-enolates were prepared from carbonyl compounds, and reacted with amines in the presence of an acid and a desiccant. DFT studie

Synthesis and cytotoxicity of thieno[2,3-b]quinoline-2-carboxamide and cycloalkyl[b]thieno[3,2-e]pyridine-2-carboxamide derivatives

Seventy nine derivatives of thieno[2,3-b]quinolines, tetrahydrothieno[2,3-b]quinoline, dihydrocyclopenta[b]thieno[3,2-e]pyridine, cyclohepta[b]thieno[3,2-e]pyridine and hexahydrocycloocta[b]thieno[3,2-e]pyridine were either synthesized or obtained commercially and tested for their antiproliferative activity against HCT116, MDA-MB-468 and MDA-MB-231 human cancer cell lines. The most potent eight compounds were active against all cell lines with IC50 values in the 80–250 nM range. In general hexahydrocycloocta[b]thieno[3,2-e]pyridines were most active with increasing activity observed as larger cycloalkyl rings were fused to the pyridine ring.

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