Cas 52811-49-1,3-Pyridinecarboxylic acid,1,4-dihydro-5-(1-hydroxyethyl)-4-(9Hpyrido[ 3,4-b]indol-1-ylmethyl)-,methyl ester

52811-49-1

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Basic information

Product Name: 3-Pyridinecarboxylic acid,1,4-dihydro-5-(1-hydroxyethyl)-4-(9Hpyrido[ 3,4-b]indol-1-ylmethyl)-,methyl ester
Synonyms:
CAS NO:52811-49-1
Molecular Formula:
Molecular Weight: 363.416
EINECS: N/A
Product Categories: N/A
Mol File: 52811-49-1.mol

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: 3-Pyridinecarboxylic acid,1,4-dihydro-5-(1-hydroxyethyl)-4-(9Hpyrido[ 3,4-b]indol-1-ylmethyl)-,methyl ester (CAS DataBase Reference)
NIST Chemistry Reference: 3-Pyridinecarboxylic acid,1,4-dihydro-5-(1-hydroxyethyl)-4-(9Hpyrido[ 3,4-b]indol-1-ylmethyl)-,methyl ester (52811-49-1)
EPA Substance Registry System: 3-Pyridinecarboxylic acid,1,4-dihydro-5-(1-hydroxyethyl)-4-(9Hpyrido[ 3,4-b]indol-1-ylmethyl)-,methyl ester (52811-49-1)

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: 52811-49-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 52811-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52811-49:
(7*5)+(6*2)+(5*8)+(4*1)+(3*1)+(2*4)+(1*9)=111
111 % 10 = 1
So 52811-49-1 is a valid CAS Registry Number.

52811-49-1Upstream product

668987-16-4 methyl 5-acetyl-4-[(β-carbolin-1-yl)methyl]-1,4-dihydropyridine-3-carboxylate

52811-49-1Downstream Products

52811-49-1Relevant academic research and scientific papers

Total Synthesis of the Proposed Structures of Indole Alkaloids Lyaline and Lyadine

Bennasar, M.-Lluisa,Roca, Tomas,Monerris, Manuel

, p. 752 - 756 (2004)

The harman-1,4-dihydropyridines 1 and 2, which constitute the originally proposed structures for the indole alkaloids lyaline and lyadine, have been synthesized, and their NMR data have been compared with those available for the natural products. Due to the discrepancies in the spectral data, the structures of lyadine and lyaline should be revised.

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