Cas 1454837-41-2,(4aR,5R,10bS)-2-(4-chlorophenyl)-5-phenyl-4a,5,6,10b-tetrahydro-4H-pyrano[3,4-c]quinolin-4-one

1454837-41-2

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Basic information

Product Name: (4aR,5R,10bS)-2-(4-chlorophenyl)-5-phenyl-4a,5,6,10b-tetrahydro-4H-pyrano[3,4-c]quinolin-4-one
Synonyms: (4aR,5R,10bS)-2-(4-chlorophenyl)-5-phenyl-4a,5,6,10b-tetrahydro-4H-pyrano[3,4-c]quinolin-4-one
CAS NO:1454837-41-2
Molecular Formula:
Molecular Weight: 387.865
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: (4aR,5R,10bS)-2-(4-chlorophenyl)-5-phenyl-4a,5,6,10b-tetrahydro-4H-pyrano[3,4-c]quinolin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,5R,10bS)-2-(4-chlorophenyl)-5-phenyl-4a,5,6,10b-tetrahydro-4H-pyrano[3,4-c]quinolin-4-one(1454837-41-2)
EPA Substance Registry System: (4aR,5R,10bS)-2-(4-chlorophenyl)-5-phenyl-4a,5,6,10b-tetrahydro-4H-pyrano[3,4-c]quinolin-4-one(1454837-41-2)

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: 1454837-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1454837-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,8,3 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1454837-41:
(9*1)+(8*4)+(7*5)+(6*4)+(5*8)+(4*3)+(3*7)+(2*4)+(1*1)=182
182 % 10 = 2
So 1454837-41-2 is a valid CAS Registry Number.

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1454837-41-2Relevant academic research and scientific papers

N-heterocyclic carbene-catalyzed stereoselective cascade reaction: Synthesis of functionalized tetrahydroquinolines

Zhang, Hai-Rui,Dong, Zhen-Wen,Yang, Yu-Jie,Wang, Ping-Luan,Hui, Xin-Ping

supporting information, p. 4750 - 4753 (2013/10/08)

The first N-heterocyclic carbene-catalyzed stereoselective aza-Michael-Michael-lactonization cascade reaction of 2′-aminophenylenones and 2-bromoenals for the construction of chiral functionalized tetrahydroquinolines with three consecutive stereogenic ce

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