Cas 159391-75-0,(5S,6S)-5-Benzyl-4-oxo-3-((S)-1-phenyl-ethyl)-6-propyl-tetrahydro-pyrimidine-1-carboxylic acid benzyl ester

159391-75-0

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Basic information

Product Name: (5S,6S)-5-Benzyl-4-oxo-3-((S)-1-phenyl-ethyl)-6-propyl-tetrahydro-pyrimidine-1-carboxylic acid benzyl ester
Synonyms: (5S,6S)-5-Benzyl-4-oxo-3-((S)-1-phenyl-ethyl)-6-propyl-tetrahydro-pyrimidine-1-carboxylic acid benzyl ester
CAS NO:159391-75-0
Molecular Formula:
Molecular Weight: 470.612
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: (5S,6S)-5-Benzyl-4-oxo-3-((S)-1-phenyl-ethyl)-6-propyl-tetrahydro-pyrimidine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5S,6S)-5-Benzyl-4-oxo-3-((S)-1-phenyl-ethyl)-6-propyl-tetrahydro-pyrimidine-1-carboxylic acid benzyl ester(159391-75-0)
EPA Substance Registry System: (5S,6S)-5-Benzyl-4-oxo-3-((S)-1-phenyl-ethyl)-6-propyl-tetrahydro-pyrimidine-1-carboxylic acid benzyl ester(159391-75-0)

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: 159391-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 159391-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,3,9 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 159391-75:
(8*1)+(7*5)+(6*9)+(5*3)+(4*9)+(3*1)+(2*7)+(1*5)=170
170 % 10 = 0
So 159391-75-0 is a valid CAS Registry Number.

159391-75-0Upstream product

159391-75-0Downstream Products

159391-79-4 (2S,3S)-2-Benzyl-3-aminohexanoic acid

159391-75-0Relevant academic research and scientific papers

Highly diastereoselective alkylation of perhydropyrimidin-4-ones directed toward the synthesis of α-substituted β-amino acids. 2

Braschi,Cardillo,Tomasini,Venezia

, p. 7292 - 7298 (2007/10/02)

The alkylation of several enantiomerically pure perhydropyrimidin-4-ones at C5 is described. For the methylation reaction, mixtures of 5,6-trans -and cis-disubstituted adducts were obtained with high diastereomeric ratios, whereas only the 5,6-

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