90493-97-3

Basic information

• Product Name: Ethanone, 2-chloro-1-(2,2-dimethyl-1,3-dioxolan-4-yl)- (9CI)
• Synonyms: Ethanone, 2-chloro-1-(2,2-dimethyl-1,3-dioxolan-4-yl)- (9CI)
• CAS NO: 90493-97-3
• Molecular Formula: C7H11ClO3
• Molecular Weight: 178.61344
• Product Categories: ACETYLHALIDE
• Mol File: 90493-97-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanone, 2-chloro-1-(2,2-dimethyl-1,3-dioxolan-4-yl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-chloro-1-(2,2-dimethyl-1,3-dioxolan-4-yl)- (9CI)(90493-97-3)
• EPA Substance Registry System: Ethanone, 2-chloro-1-(2,2-dimethyl-1,3-dioxolan-4-yl)- (9CI)(90493-97-3)

Safety Data

• Hazardous Substances Data: 90493-97-3(Hazardous Substances Data)

Upstream product

• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 85364-08-5 (R)-4-(2,2-Dichloro-1-methoxy-ethyl)-2,2-dimethyl-[1,3]dioxolane 
• 593-71-5 Chloroiodomethane 
• 52373-72-5 methyl (R)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 
• 85364-09-6 (R)-4-((Z)-2-Chloro-1-methoxy-vinyl)-2,2-dimethyl-[1,3]dioxolane 
• 60456-21-5 methyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 
• 22323-80-4 (4S)-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 85364-08-5 (S)-4-(2,2-Dichloro-1-methoxy-ethyl)-2,2-dimethyl-[1,3]dioxolane 
• 85364-09-6 (S)-4-((Z)-2-Chloro-1-methoxy-vinyl)-2,2-dimethyl-[1,3]dioxolane 

Relevant articles and documents

FUSED TRICYCLIC IMIDAZOLE DERIVATIVES AS MODULATORS OF TNF ACTIVITY

A series of substituted fused tricyclic imidazole derivatives, in particular dihydro- 1H-pyrano[4',3':4,5]imidazo[1,2-a]pyridine, 1,2,3,4-tetrahydroimidazo[1,2-a:5,4- c']dipyridine, dihydro-1H-pyrano[3',4':4,5]imidazo[1,2-a]pyridine and tetrahydro-6H- cyc

Single-step synthesis of cyclopentenones from (3-alkoxycarbonyl-2-oxopropylidene)triphenylphosphorane and 1,2-diacylethylenes

(3-Alkoxycarbonyl-2-oxo-propylidene)triphenylphosphorane reacts with 1,2-diacylethylenes to give cyclopentenones in a single operation. Use of a chiral acylmethylenemalonate led to formation of optically active cyclopentenone in a highly diastereoselectiv