Cas 205437-40-7,(2E,4S)-2,2-dimethyl-3-(2-methyl-1-oxo-2-butenyl)-4-phenylmethyloxazolidine

205437-40-7

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Basic information

Product Name: (2E,4S)-2,2-dimethyl-3-(2-methyl-1-oxo-2-butenyl)-4-phenylmethyloxazolidine
Synonyms: (2E,4S)-2,2-dimethyl-3-(2-methyl-1-oxo-2-butenyl)-4-phenylmethyloxazolidine
CAS NO:205437-40-7
Molecular Formula:
Molecular Weight: 273.375
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2E,4S)-2,2-dimethyl-3-(2-methyl-1-oxo-2-butenyl)-4-phenylmethyloxazolidine(CAS DataBase Reference)
NIST Chemistry Reference: (2E,4S)-2,2-dimethyl-3-(2-methyl-1-oxo-2-butenyl)-4-phenylmethyloxazolidine(205437-40-7)
EPA Substance Registry System: (2E,4S)-2,2-dimethyl-3-(2-methyl-1-oxo-2-butenyl)-4-phenylmethyloxazolidine(205437-40-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 205437-40-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 205437-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,4,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 205437-40:
(8*2)+(7*0)+(6*5)+(5*4)+(4*3)+(3*7)+(2*4)+(1*0)=107
107 % 10 = 7
So 205437-40-7 is a valid CAS Registry Number.

205437-40-7Upstream product

205437-40-7Downstream Products

205437-40-7Relevant academic research and scientific papers

Opposite π-face selectivity for the DMD and m-CPBA epoxidations of chiral 2,2-dimethyloxazolidine derivatives of tiglic amides: Control by steric interactions versus hydrogen bonding

Adam, Waldemar,Pastor, Aurelia,Peters, Karl,Peters, Eva-Maria

, p. 1019 - 1022 (2007/10/03)

A high extent but opposite sense in the diastereoselectivity has been observed for the DMD and m-CPBA epoxidations of the optically active tiglic amides (S)-1 with 2,2-dimethyloxazolidines as chiral auxiliaries. This unprecedented reversed π-facial differ

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