Cas 401613-62-5,(4S,4'S)-3-(4'-benzyl-2'-thioxo-1',3'-thiazolidine-3'-carbonyl)-4-(1-methoxycarbonyl-1-methylethyl)-4H-pyridine-1-carboxylic acid methyl ester

401613-62-5

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Basic information

Product Name: (4S,4'S)-3-(4'-benzyl-2'-thioxo-1',3'-thiazolidine-3'-carbonyl)-4-(1-methoxycarbonyl-1-methylethyl)-4H-pyridine-1-carboxylic acid methyl ester
Synonyms:
CAS NO:401613-62-5
Molecular Formula:
Molecular Weight: 474.602
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: (4S,4'S)-3-(4'-benzyl-2'-thioxo-1',3'-thiazolidine-3'-carbonyl)-4-(1-methoxycarbonyl-1-methylethyl)-4H-pyridine-1-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4S,4'S)-3-(4'-benzyl-2'-thioxo-1',3'-thiazolidine-3'-carbonyl)-4-(1-methoxycarbonyl-1-methylethyl)-4H-pyridine-1-carboxylic acid methyl ester(401613-62-5)
EPA Substance Registry System: (4S,4'S)-3-(4'-benzyl-2'-thioxo-1',3'-thiazolidine-3'-carbonyl)-4-(1-methoxycarbonyl-1-methylethyl)-4H-pyridine-1-carboxylic acid methyl ester(401613-62-5)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 401613-62-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 401613-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,6,1 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 401613-62:
(8*4)+(7*0)+(6*1)+(5*6)+(4*1)+(3*3)+(2*6)+(1*2)=95
95 % 10 = 5
So 401613-62-5 is a valid CAS Registry Number.

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401613-62-5Relevant academic research and scientific papers

Regio- and stereoselective synthesis of 1,4-dihydropyridines by way of an intramolecular interaction of a thiocarbonyl or carbonyl with a pyridinium nucleus

Yamada, Shinji,Misono, Tomoko,Ichikawa, Mayumi,Morita, Chisako

, p. 8939 - 8949 (2007/10/03)

Chiral 1,4-dihydropyridines were prepared by the regio- and stereoselective addition of ketene silyl acetals and organometallic reagents to pyridinium salts. In the addition reaction, an intramolecular interaction between the thiocarbonyl or carbonyl with

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