Cas 1215007-33-2,(2S,4R)-3-[(2R,3R)-3-hydroxy-2-methyl-3-phenylpropanoyl]-4-phenyl-2-trifluoromethyloxazolidine

1215007-33-2

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Basic information

Product Name: (2S,4R)-3-[(2R,3R)-3-hydroxy-2-methyl-3-phenylpropanoyl]-4-phenyl-2-trifluoromethyloxazolidine
Synonyms: (2S,4R)-3-[(2R,3R)-3-hydroxy-2-methyl-3-phenylpropanoyl]-4-phenyl-2-trifluoromethyloxazolidine
CAS NO:1215007-33-2
Molecular Formula:
Molecular Weight: 379.379
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: (2S,4R)-3-[(2R,3R)-3-hydroxy-2-methyl-3-phenylpropanoyl]-4-phenyl-2-trifluoromethyloxazolidine(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4R)-3-[(2R,3R)-3-hydroxy-2-methyl-3-phenylpropanoyl]-4-phenyl-2-trifluoromethyloxazolidine(1215007-33-2)
EPA Substance Registry System: (2S,4R)-3-[(2R,3R)-3-hydroxy-2-methyl-3-phenylpropanoyl]-4-phenyl-2-trifluoromethyloxazolidine(1215007-33-2)

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: 1215007-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1215007-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,5,0,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1215007-33:
(9*1)+(8*2)+(7*1)+(6*5)+(5*0)+(4*0)+(3*7)+(2*3)+(1*3)=92
92 % 10 = 2
So 1215007-33-2 is a valid CAS Registry Number.

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1215007-33-2Relevant academic research and scientific papers

Asymmetric aldol reactions using chiral CF3-Oxazolidines (Fox) as chiral auxiliary

Tessier, Arnaud,Pytkowicz, Julien,Brigaud, Thierry

experimental part, p. 1140 - 1144 (2010/03/02)

The aldol reactions of amide enolates derived from a trifluoromethylated oxazolidine (Fox) chiral auxiliary occur in good yields with a moderate anti diastereoselectivity (Li and Na enolates) to a high syn diastereoselectivity (boron enolate). After remov

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