Cas 141436-35-3,(3R,5S)-5-Benzyl-3-((R)-hydroxy-phenyl-methyl)-2-oxo-morpholine-4-carboxylic acid tert-butyl ester

141436-35-3

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Basic information

Product Name: (3R,5S)-5-Benzyl-3-((R)-hydroxy-phenyl-methyl)-2-oxo-morpholine-4-carboxylic acid tert-butyl ester
Synonyms:
CAS NO:141436-35-3
Molecular Formula:
Molecular Weight: 397.471
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: (3R,5S)-5-Benzyl-3-((R)-hydroxy-phenyl-methyl)-2-oxo-morpholine-4-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3R,5S)-5-Benzyl-3-((R)-hydroxy-phenyl-methyl)-2-oxo-morpholine-4-carboxylic acid tert-butyl ester(141436-35-3)
EPA Substance Registry System: (3R,5S)-5-Benzyl-3-((R)-hydroxy-phenyl-methyl)-2-oxo-morpholine-4-carboxylic acid tert-butyl ester(141436-35-3)

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: 141436-35-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141436-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,3 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141436-35:
(8*1)+(7*4)+(6*1)+(5*4)+(4*3)+(3*6)+(2*3)+(1*5)=103
103 % 10 = 3
So 141436-35-3 is a valid CAS Registry Number.

141436-35-3Upstream product

141436-35-3Downstream Products

141436-35-3Relevant academic research and scientific papers

Synthesis and Structure Determination of (3S,5S)-2,3,5,6-Tetrahydro-3,5-dialkyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazine-2-ones

Baker, William R.,Condon, Stephen L.,Spanton, Stephen

, p. 1573 - 1576 (1992)

(5S)-2,3,5,6-Tetrahydro-5-alkyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazine-2-ones, which are readily prepared from optically pure 2-amino alcohols alkylate selectively at the C-3 position to give (3S,5S)-dialkyl-2,3,5,6-tetrahydro-5-alkyl-N-(tert-butyloxyca

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