Cas 194491-68-4,1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-5-[[octahydro-3-oxo-1-(phenylmethyl)-2-azocinyl]methyl]-, methyl ester

194491-68-4

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Basic information

Product Name: 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-5-[[octahydro-3-oxo-1-(phenylmethyl)-2-azocinyl]methyl]-, methyl ester
Synonyms:
CAS NO:194491-68-4
Molecular Formula: C22H30N2O3
Molecular Weight: 370.492
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: 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-5-[[octahydro-3-oxo-1-(phenylmethyl)-2-azocinyl]methyl]-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-5-[[octahydro-3-oxo-1-(phenylmethyl)-2-azocinyl]methyl]-, methyl ester(194491-68-4)
EPA Substance Registry System: 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-5-[[octahydro-3-oxo-1-(phenylmethyl)-2-azocinyl]methyl]-, methyl ester(194491-68-4)

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: 194491-68-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 194491-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,4,9 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 194491-68:
(8*1)+(7*9)+(6*4)+(5*4)+(4*9)+(3*1)+(2*6)+(1*8)=174
174 % 10 = 4
So 194491-68-4 is a valid CAS Registry Number.

194491-68-4Upstream product

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194491-68-4Relevant academic research and scientific papers

A HIGHLY STEREOSELECTIVE APPROACH TO THE SYNTHESIS OF THE MANZAMINE ALKALOIDS VIA THE INTRAMOLECULAR VINYLOGOUS AMIDE PHOTOCYCLOADDITION

Winkler, Jeffrey D.,Siegel, Miles G.,Stelmach, John E.

, p. 6509 - 6512 (1993)

The stereoselective construction of the tetracyclic core of the manzamine alkaloids via the intramolecular vinylogous amide photocycloaddition/retro-Mannich fragmentation/Mannich closure sequence using an eight-membered ring template is described.

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