Cas 139259-19-1,1H-Indole-3-propanoic acid, a-(3,4-dihydro-4-oxo-1(2H)-pyridinyl)-1-[(phenylmethoxy)carbonyl]-, methyl ester, (S)-

139259-19-1

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Basic information

Product Name: 1H-Indole-3-propanoic acid, a-(3,4-dihydro-4-oxo-1(2H)-pyridinyl)-1-[(phenylmethoxy)carbonyl]-, methyl ester, (S)-
Synonyms:
CAS NO:139259-19-1
Molecular Formula: C25H24N2O5
Molecular Weight: 432.476
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: 1H-Indole-3-propanoic acid, a-(3,4-dihydro-4-oxo-1(2H)-pyridinyl)-1-[(phenylmethoxy)carbonyl]-, methyl ester, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole-3-propanoic acid, a-(3,4-dihydro-4-oxo-1(2H)-pyridinyl)-1-[(phenylmethoxy)carbonyl]-, methyl ester, (S)-(139259-19-1)
EPA Substance Registry System: 1H-Indole-3-propanoic acid, a-(3,4-dihydro-4-oxo-1(2H)-pyridinyl)-1-[(phenylmethoxy)carbonyl]-, methyl ester, (S)-(139259-19-1)

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: 139259-19-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139259-19-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,5 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 139259-19:
(8*1)+(7*3)+(6*9)+(5*2)+(4*5)+(3*9)+(2*1)+(1*9)=151
151 % 10 = 1
So 139259-19-1 is a valid CAS Registry Number.

139259-19-1Upstream product

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139259-19-1Relevant academic research and scientific papers

Asymmetric Synthesis of Indoloquinolizidin-2-ones Congeners to Yohimbine-Type Alkaloids

Waldmann, Herbert,Braun, Matthias,Weymann, Markus,Gewehr, Markus

, p. 397 - 416 (1993)

Schiff bases derived from tryptophan methyl ester and tryptamine react with Danishefkys diene in the presence of ZnCl2 to give enaminones which are subsequently transformed into indoloquinolizidin-2-ones by acid-catalyzed cyclization.These tetracyc

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