81102-65-0

Basic information

• Product Name: (S)-2,2-Dimethyl-4-(2-methyl-3-nitro-phenoxymethyl)-[1,3]dioxolane
• Synonyms: (S)-2,2-Dimethyl-4-(2-methyl-3-nitro-phenoxymethyl)-[1,3]dioxolane
• CAS NO: 81102-65-0
• Molecular Weight: 267.282
• Mol File: 81102-65-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2,2-Dimethyl-4-(2-methyl-3-nitro-phenoxymethyl)-[1,3]dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2,2-Dimethyl-4-(2-methyl-3-nitro-phenoxymethyl)-[1,3]dioxolane(81102-65-0)
• EPA Substance Registry System: (S)-2,2-Dimethyl-4-(2-methyl-3-nitro-phenoxymethyl)-[1,3]dioxolane(81102-65-0)

Safety Data

• Hazardous Substances Data: 81102-65-0(Hazardous Substances Data)

Upstream product

• 5460-31-1 3-nitro-o-cresol 
• 23788-74-1 (R)-2,2-dimethyl-1,3-dioxolane-4-ylmethyl p-toluenesulfonate 
• 1707-77-3 1,2:5,6-di-O-isopropylidene-D-mannitol 
• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 22323-82-6 (S)-(+)-(2,2-dimethyl-[1,3]dioxolan-4-yl)methanol 

Downstream Products

• 81745-07-5 (R)-5-[2-((E)-2-Dimethylamino-vinyl)-3-nitro-phenoxymethyl]-3-isopropyl-oxazolidin-2-one 
• 81745-07-5 5-[2-((E)-2-Dimethylamino-vinyl)-3-nitro-phenoxymethyl]-3-isopropyl-oxazolidin-2-one 
• 81102-70-7 <5R>-3-isopropyl-5-(2-methyl-3-nitrophenoxymethyl)-oxazolidin-2-one 
• 74088-75-8 3-isopropyl-5-(2-methyl-3-nitrophenoxymethyl)-oxazolidin-2-one 
• 81132-32-3 <2R>-(+)-1-isopropylamino-3-(2-methyl-3-nitrophenoxy)-2-propanol 
• 81102-67-2 C₂₄H₂₅NO₉S₂ 
• 81102-68-3 Toluene-4-sulfonic acid (S)-2-hydroxy-3-(2-methyl-3-nitro-phenoxy)-propyl ester 
• 13523-86-9 1-(1H-indol-4-yloxy)-3-(isopropylamino)-2-propanol 
• 81102-66-1 <2R>-3-(2-methyl-3-nitrophenoxy)-1,2-propanediol 

Relevant articles and documents

Practical Syntheses of - and -1-Alkylamino-3-aryloxy-2-porpanols from a Single Carbohydrate Precursor

A practical synthetic route to optically active - and -1-alkylamino-3-aryloxy-2-propanols (β-blockers) from -2,3-O-isopropylideneglyceraldehyde (-1) was developed.Synthesis of the -isomers was carried out as follows.Borohydride reduction of -1 in the presence of excess alkylamine followed by alkoxycarbonylation, acid hydrolysis, and cyclization under K2CO3 catalysis gave -3-alkyl-5-hydroxymethyl-1,3-oxazolidin-2-ones, the tosylates of which were coupled with various phenols then hydrolyzed by alkali treatment to give -(-)-β-blockers (e.g., propranolol, carteolol) in satisfactory yields. -,-, and rac-pindolol were synthesized from the corresponding 3-isopropyl-5-(2-methyl-3-nitrophenoxymethyl)-1,3-oxazolidin-2-one by application of the Leimgruber-Batcho method.Keywords--- and -1-alkylamino-3-aryloxy-2-propanols; optically active β-blockers; propranolol; carteolol; pindolol; carbohydrate precursor; -2,3-O-isopropylideneglyceraldehyde; -3-alkyl-5-hydroxymethyl-1,3-oxazolidin-2-ones; Leimgruber-Batcho indole synthesis