Cas 1319741-35-9,(+)-(2R,4R)-tert-butyl 4-ethyl-2-(3-methylbenzyl)oxazolidine-3-carboxylate

1319741-35-9

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Basic information

Product Name: (+)-(2R,4R)-tert-butyl 4-ethyl-2-(3-methylbenzyl)oxazolidine-3-carboxylate
Synonyms: (+)-(2R,4R)-tert-butyl 4-ethyl-2-(3-methylbenzyl)oxazolidine-3-carboxylate
CAS NO:1319741-35-9
Molecular Formula:
Molecular Weight: 305.417
EINECS: N/A
Product Categories: N/A
Mol File: 1319741-35-9.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: (+)-(2R,4R)-tert-butyl 4-ethyl-2-(3-methylbenzyl)oxazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (+)-(2R,4R)-tert-butyl 4-ethyl-2-(3-methylbenzyl)oxazolidine-3-carboxylate(1319741-35-9)
EPA Substance Registry System: (+)-(2R,4R)-tert-butyl 4-ethyl-2-(3-methylbenzyl)oxazolidine-3-carboxylate(1319741-35-9)

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: 1319741-35-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1319741-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,9,7,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1319741-35:
(9*1)+(8*3)+(7*1)+(6*9)+(5*7)+(4*4)+(3*1)+(2*3)+(1*5)=159
159 % 10 = 9
So 1319741-35-9 is a valid CAS Registry Number.

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1319741-35-9Relevant articles and documents

Stereoselective synthesis of substituted 1,3-oxazolidines via Pd-catalyzed carboamination reactions of o-vinyl-1,2-amino alcohols

Ward, Amanda F.,Wolfe, John P.

, p. 4728 - 4731 (2011/10/13)

The stereoselective synthesis of 2,4- and 2,5-disubstituted 1,3-oxazolidines is accomplished via Pd-catalyzed carboamination of O-vinyl-1,2-amino alcohol derivatives. The transformations generate cis-disubstituted products with good to excellent diastereo

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