Cas 141075-65-2,(S)-2-((4S,5S)-5-Methyl-4-methylcarbamoyl-4,5-dihydro-oxazol-2-yl)-pyrrolidine-1-carboxylic acid benzyl ester

141075-65-2

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Basic information

Product Name: (S)-2-((4S,5S)-5-Methyl-4-methylcarbamoyl-4,5-dihydro-oxazol-2-yl)-pyrrolidine-1-carboxylic acid benzyl ester
Synonyms:
CAS NO:141075-65-2
Molecular Formula:
Molecular Weight: 345.398
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: (S)-2-((4S,5S)-5-Methyl-4-methylcarbamoyl-4,5-dihydro-oxazol-2-yl)-pyrrolidine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((4S,5S)-5-Methyl-4-methylcarbamoyl-4,5-dihydro-oxazol-2-yl)-pyrrolidine-1-carboxylic acid benzyl ester(141075-65-2)
EPA Substance Registry System: (S)-2-((4S,5S)-5-Methyl-4-methylcarbamoyl-4,5-dihydro-oxazol-2-yl)-pyrrolidine-1-carboxylic acid benzyl ester(141075-65-2)

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: 141075-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141075-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,7 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141075-65:
(8*1)+(7*4)+(6*1)+(5*0)+(4*7)+(3*5)+(2*6)+(1*5)=102
102 % 10 = 2
So 141075-65-2 is a valid CAS Registry Number.

141075-65-2Upstream product

141075-65-2Downstream Products

141075-65-2Relevant academic research and scientific papers

A short, stereospecific synthesis of dihydrooxazoles from serine and threonine derivatives

Wipf, Peter,Miller, Chris P.

, p. 907 - 910 (2007/10/02)

Cyclization of serine and threonine derivatives with Burgess reagent provides a one-step, streospecific access to 4,5-dihydrooxazoles. Noteworthy features of this new methodology include mild experimental conditions, and the absence of β-lactam, aziridine

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