66574-19-4

Basic information

• Product Name: 3,4－Dimethyl－5－phenyloxazolidine
• Synonyms: 3,4－Dimethyl－5－phenyloxazolidine
• CAS NO: 66574-19-4
• Molecular Formula: C₁₁H₁₅NO
• Molecular Weight: 177.2429
• Mol File: 66574-19-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 256.9°C at 760 mmHg
• Flash Point: 75.2°C
• Appearance: /
• Density: 1.012g/cm³
• Vapor Pressure: 0.015mmHg at 25°C
• Refractive Index: 1.516
• CAS DataBase Reference: 3,4－Dimethyl－5－phenyloxazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4－Dimethyl－5－phenyloxazolidine(66574-19-4)
• EPA Substance Registry System: 3,4－Dimethyl－5－phenyloxazolidine(66574-19-4)

Safety Data

• Hazardous Substances Data: 66574-19-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H15NO/c1-9-11(13-8-12(9)2)10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3

Upstream product

• 50-00-0 formaldehyd 
• 90-82-4 rac-pseudoephedrine 
• 90-81-3 ephedrine 
• 1047392-28-8 methyl 2-(N-acetylamino)-5-ethynylbenzoate 
• 90-82-4 pseudoephedrine 
• 74-95-3 1,1-dibromomethane 
• 75-09-2 dichloromethane 

Downstream Products

• 462871-59-6 {[((1S,2S)-2-Chloro-1-methyl-2-phenyl-ethyl)-methyl-amino]-methyl}-phosphonic acid diethyl ester 
• 462871-75-6 ((2S,3R,4S)-1,4-Dimethyl-3-phenyl-azetidin-2-yl)-phosphonic acid diethyl ester 
• 462871-44-9 {[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amino]-methyl}-phosphonic acid diethyl ester 
• 1201-56-5 (1S,2S)-N-Methylpseudoephedrine 

Relevant articles and documents

Study of alkaloids of the Siberian and Altai flora 14. Synthesis of alkaloid-based tertiary N-(3-arylprop-2-ynyl)amines

3-Arylprop-2-ynylamines containing the key fragment of known alkaloids of the Altai flora were synthesized by the Sonogashira and Mannich reactions.

An efficient asymmetric synthesis of azetidine 2-phosphonic acids

Substituted azetidinic 2-phosphonates were prepared in diastereoisomerically and enantiomerically pure form, starting from readily available β-amino alcohols. This synthesis involved a three-step sequence: (i) N-alkylation of the starting amino alcohol wi

The solid-state diastereoselective formation of oxazolidines

A number of organic and organometallic aldehydes have been converted into optically active oxazolidines by solid-state interaction with (-)-ephedrine and (+)-pseudoephedrine. The stereoselectivity of the solid-state reaction is compared with that in boili