Cas 1186398-99-1,(2S,4R)-N-benzoyl-2-tert-butyl-4-(methyl-d3)-4-methyloxazolidin-5-one

1186398-99-1

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Basic information

Product Name: (2S,4R)-N-benzoyl-2-tert-butyl-4-(methyl-d3)-4-methyloxazolidin-5-one
Synonyms: (2S,4R)-N-benzoyl-2-tert-butyl-4-(methyl-d3)-4-methyloxazolidin-5-one
CAS NO:1186398-99-1
Molecular Formula:
Molecular Weight: 278.324
EINECS: N/A
Product Categories: N/A
Mol File: 1186398-99-1.mol
Article Data: 1

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)-N-benzoyl-2-tert-butyl-4-(methyl-d3)-4-methyloxazolidin-5-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4R)-N-benzoyl-2-tert-butyl-4-(methyl-d3)-4-methyloxazolidin-5-one(1186398-99-1)
EPA Substance Registry System: (2S,4R)-N-benzoyl-2-tert-butyl-4-(methyl-d3)-4-methyloxazolidin-5-one(1186398-99-1)

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: 1186398-99-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1186398-99-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,6,3,9 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1186398-99:
(9*1)+(8*1)+(7*8)+(6*6)+(5*3)+(4*9)+(3*8)+(2*9)+(1*9)=211
211 % 10 = 1
So 1186398-99-1 is a valid CAS Registry Number.

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1186398-99-1Relevant articles and documents

Asymmetric autocatalysis induced by meteoritic amino acids with hydrogen isotope chirality

Kawasaki, Tsuneomi,Shimizu, Masako,Nishiyama, Daisuke,Ito, Masateru,Ozawa, Hitomi,Soai, Kenso

supporting information; experimental part, p. 4396 - 4398 (2010/01/16)

Achiral meteoritic amino acids, glycine and α-methylalanine, with hydrogen isotope (D/H) chirality, acted as the source of chirality in asymmetric autocatalysis with amplification of ee to afford highly enantioenriched 5-pyrimidyl alkanols. The Royal Soci

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