Cas 1200953-79-2,(3S)-3-[(2S)-1-(tert-butyloxycarbonyl)tetrahydro-1H-2-pyrrolyl]carboxamido-4-phenylbutanoic acid methyl ester

1200953-79-2

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Basic information

Product Name: (3S)-3-[(2S)-1-(tert-butyloxycarbonyl)tetrahydro-1H-2-pyrrolyl]carboxamido-4-phenylbutanoic acid methyl ester
Synonyms: (3S)-3-[(2S)-1-(tert-butyloxycarbonyl)tetrahydro-1H-2-pyrrolyl]carboxamido-4-phenylbutanoic acid methyl ester
CAS NO:1200953-79-2
Molecular Formula:
Molecular Weight: 390.48
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: (3S)-3-[(2S)-1-(tert-butyloxycarbonyl)tetrahydro-1H-2-pyrrolyl]carboxamido-4-phenylbutanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3S)-3-[(2S)-1-(tert-butyloxycarbonyl)tetrahydro-1H-2-pyrrolyl]carboxamido-4-phenylbutanoic acid methyl ester(1200953-79-2)
EPA Substance Registry System: (3S)-3-[(2S)-1-(tert-butyloxycarbonyl)tetrahydro-1H-2-pyrrolyl]carboxamido-4-phenylbutanoic acid methyl ester(1200953-79-2)

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: 1200953-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1200953-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,0,9,5 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1200953-79:
(9*1)+(8*2)+(7*0)+(6*0)+(5*9)+(4*5)+(3*3)+(2*7)+(1*9)=122
122 % 10 = 2
So 1200953-79-2 is a valid CAS Registry Number.

1200953-79-2Upstream product

1200953-79-2Downstream Products

1200953-41-8 (3S)-4-phenyl-3-[(2S)-tetrahydro-1H-2-pyrrolylcarboxamido]butanoic acid methyl ester

1200953-79-2Relevant academic research and scientific papers

Proline-β3-amino-ester dipeptides as efficient catalysts for enantioselective direct aldol reaction in aqueous medium

De Nisco, Mauro,Pedatella, Silvana,Ullah, Hidayat,Zaidi, Javid H.,Naviglio, Daniele,Oezdamar, Oezguer,Caputo, Romualdo

, p. 9562 - 9565 (2009)

(Chemical Equation Presented) Dipeptides obtained from L-proline and β3-L-amino acids are reported to catalyze enantioselective direct aldol reaction in aqueous medium, leading to significant anti: syn diastereomeric ratios and enantiomeric exc

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