Cas 223505-38-2,(4S,5S)-5-Methyl-4-((S)-2-oxo-piperidin-4-yl)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester

223505-38-2

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Basic information

Product Name: (4S,5S)-5-Methyl-4-((S)-2-oxo-piperidin-4-yl)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester
Synonyms: (4S,5S)-5-Methyl-4-((S)-2-oxo-piperidin-4-yl)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester
CAS NO:223505-38-2
Molecular Formula:
Molecular Weight: 316.357
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: (4S,5S)-5-Methyl-4-((S)-2-oxo-piperidin-4-yl)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5S)-5-Methyl-4-((S)-2-oxo-piperidin-4-yl)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester(223505-38-2)
EPA Substance Registry System: (4S,5S)-5-Methyl-4-((S)-2-oxo-piperidin-4-yl)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester(223505-38-2)

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: 223505-38-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 223505-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,5,0 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 223505-38:
(8*2)+(7*2)+(6*3)+(5*5)+(4*0)+(3*5)+(2*3)+(1*8)=102
102 % 10 = 2
So 223505-38-2 is a valid CAS Registry Number.

223505-38-2Upstream product

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223505-38-2Relevant academic research and scientific papers

Studies towards a total synthesis of Sarains A-C. Stereospecific condensation of α,β-unsaturated esters with the phenyl oxazoline derivative of threonine

Jaroch, Stefan,Matsuoka, Richard T.,Overman, Larry E.

, p. 1273 - 1276 (2007/10/03)

Michael addition of oxazoline lithium enolate 5 to E and Z α,β- unsaturated esters proceeds with high enoate facial selectivity to yield enantiopure oxazoline derivatives of disubstituted glutamic acids. When a Z enoate is employed, the C4'-C3'-C7' stereo

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