Cas 261963-27-3,(-)-(R)-(phenyl)(phenylmethoxycarbonylamino)acetic acid 3,3-dimethyl-2-oxo-butyl ester

261963-27-3

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Basic information

Product Name: (-)-(R)-(phenyl)(phenylmethoxycarbonylamino)acetic acid 3,3-dimethyl-2-oxo-butyl ester
Synonyms: (-)-(R)-(phenyl)(phenylmethoxycarbonylamino)acetic acid 3,3-dimethyl-2-oxo-butyl ester
CAS NO:261963-27-3
Molecular Formula:
Molecular Weight: 383.444
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: (-)-(R)-(phenyl)(phenylmethoxycarbonylamino)acetic acid 3,3-dimethyl-2-oxo-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(R)-(phenyl)(phenylmethoxycarbonylamino)acetic acid 3,3-dimethyl-2-oxo-butyl ester(261963-27-3)
EPA Substance Registry System: (-)-(R)-(phenyl)(phenylmethoxycarbonylamino)acetic acid 3,3-dimethyl-2-oxo-butyl ester(261963-27-3)

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: 261963-27-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 261963-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,9,6 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 261963-27:
(8*2)+(7*6)+(6*1)+(5*9)+(4*6)+(3*3)+(2*2)+(1*7)=153
153 % 10 = 3
So 261963-27-3 is a valid CAS Registry Number.

261963-27-3Upstream product

5469-26-1 1-Bromopinacolon

261963-27-3Downstream Products

261963-27-3Relevant academic research and scientific papers

A general synthesis of enantiopure 1,2-aminoalcohols via chiral morpholinones

Segat-Dioury, Fabienne,Lingibé, Olivier,Graffe, Bernadette,Sacquet, Marie-Claude,Lhommet, Gérard

, p. 233 - 248 (2007/10/03)

Eleven optically active 1,2-aminoalcohols 20a-i and 26b-c were prepared from D-phenylglycine via cyclic imines 7b-i (or enamine 7a). The key step of the strategy is the diastereoselective reduction of chiral oxazinones 7a-i.

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