Cas 1380402-64-1,(3S,4R)-4,6-diphenyl-3-(thiophen-2-yl)-1-tosyl-3,4-dihydropyridin-2(1H)-one

1380402-64-1

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Basic information

Product Name: (3S,4R)-4,6-diphenyl-3-(thiophen-2-yl)-1-tosyl-3,4-dihydropyridin-2(1H)-one
Synonyms: (3S,4R)-4,6-diphenyl-3-(thiophen-2-yl)-1-tosyl-3,4-dihydropyridin-2(1H)-one
CAS NO:1380402-64-1
Molecular Formula:
Molecular Weight: 485.628
EINECS: N/A
Product Categories: N/A
Mol File: 1380402-64-1.mol
Article Data: 2

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,4R)-4,6-diphenyl-3-(thiophen-2-yl)-1-tosyl-3,4-dihydropyridin-2(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-4,6-diphenyl-3-(thiophen-2-yl)-1-tosyl-3,4-dihydropyridin-2(1H)-one(1380402-64-1)
EPA Substance Registry System: (3S,4R)-4,6-diphenyl-3-(thiophen-2-yl)-1-tosyl-3,4-dihydropyridin-2(1H)-one(1380402-64-1)

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: 1380402-64-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1380402-64-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,4,0 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1380402-64:
(9*1)+(8*3)+(7*8)+(6*0)+(5*4)+(4*0)+(3*2)+(2*6)+(1*4)=131
131 % 10 = 1
So 1380402-64-1 is a valid CAS Registry Number.

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1380402-64-1Relevant articles and documents

A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow

Izquierdo, Javier,Pericàs, Miquel A.

, p. 348 - 356 (2016/01/12)

A polystyrene-supported, enantiopure benzotetramisole (BTM) analogue (5) has been synthesized from (2S,3S)-phenylglycidol through a five-step sequence involving a copper-catalyzed alkyne azide cycloaddition (CuAAC) reaction as the final, immobilization st

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