Cas 872880-48-3,Carbamic acid, [(1S,2S)-3-hydroxy-2-phenyl-1-(1-pyrrolidinylcarbonyl)propyl]-, 1,1-dimethylethyl ester

872880-48-3

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Basic information

Product Name: Carbamic acid, [(1S,2S)-3-hydroxy-2-phenyl-1-(1-pyrrolidinylcarbonyl)propyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:872880-48-3
Molecular Formula: C19H28N2O4
Molecular Weight: 348.442
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: Carbamic acid, [(1S,2S)-3-hydroxy-2-phenyl-1-(1-pyrrolidinylcarbonyl)propyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S,2S)-3-hydroxy-2-phenyl-1-(1-pyrrolidinylcarbonyl)propyl]-, 1,1-dimethylethyl ester(872880-48-3)
EPA Substance Registry System: Carbamic acid, [(1S,2S)-3-hydroxy-2-phenyl-1-(1-pyrrolidinylcarbonyl)propyl]-, 1,1-dimethylethyl ester(872880-48-3)

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: 872880-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872880-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,8,8 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 872880-48:
(8*8)+(7*7)+(6*2)+(5*8)+(4*8)+(3*0)+(2*4)+(1*8)=213
213 % 10 = 3
So 872880-48-3 is a valid CAS Registry Number.

872880-48-3Upstream product

872880-48-3Downstream Products

876955-17-8 (2S,3S)-3-tert-Butoxycarbonylamino-4-oxo-2-phenyl-4-pyrrolidin-1-yl-butyric acid

872880-48-3Relevant academic research and scientific papers

Proline-catalyzed, asymmetric Mannich reactions in the synthesis of a DPP-IV inhibitor

Janey, Jacob M.,Hsiao, Yi,Armstrong III, Joseph D.

, p. 390 - 392 (2006)

A highly stereoselective L-proline-catalyzed, asymmetric direct Mannich reaction between a glyoxalate-derived imine and phenyl acetaldehyde was employed for the formation of a syn substituted β-phenyl homoserine. This Mannich adduct was then readily elabo

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