Cas 1312716-95-2,(3S,5R)-3-carboethoxymethyl-3-trifluoromethyl-5-phenylmorpholin-2-one

1312716-95-2

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Basic information

Product Name: (3S,5R)-3-carboethoxymethyl-3-trifluoromethyl-5-phenylmorpholin-2-one
Synonyms: (3S,5R)-3-carboethoxymethyl-3-trifluoromethyl-5-phenylmorpholin-2-one
CAS NO:1312716-95-2
Molecular Formula:
Molecular Weight: 331.292
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: (3S,5R)-3-carboethoxymethyl-3-trifluoromethyl-5-phenylmorpholin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,5R)-3-carboethoxymethyl-3-trifluoromethyl-5-phenylmorpholin-2-one(1312716-95-2)
EPA Substance Registry System: (3S,5R)-3-carboethoxymethyl-3-trifluoromethyl-5-phenylmorpholin-2-one(1312716-95-2)

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: 1312716-95-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312716-95-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,1 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1312716-95:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*1)+(3*6)+(2*9)+(1*5)=132
132 % 10 = 2
So 1312716-95-2 is a valid CAS Registry Number.

1312716-95-2Upstream product

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1312716-95-2Relevant academic research and scientific papers

Concise synthesis of enantiopure (S)- and (R)-α-trifluoromethyl aspartic acid and α-trifluoromethyl serine from chiral trifluoromethyl oxazolidines (Fox) via a Strecker-type reaction

Simon, Julien,Nguyen, Thi Thuan,Chelain, Evelyne,Lensen, Nathalie,Pytkowicz, Julien,Chaume, Gregory,Brigaud, Thierry

experimental part, p. 309 - 314 (2011/05/19)

A concise synthesis of enantiopure (S)- and (R)-α-Tfm-aspartic acid and α-Tfm-serine is reported. The key step involves a Strecker-type reaction on chiral CF3-oxazolidines (Fox) derived from ethyl 4,4,4-trifluoroacetoacetate (ETFAA) or ethyl tr

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