Cas 1454837-46-7,(2R,3R,4S)-N-benzyl-4-(2-oxo-2-phenylethyl)-2-phenyl-1,2,3,4-tetrahydroquinoline-3-carboxamide

1454837-46-7

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Basic information

Product Name: (2R,3R,4S)-N-benzyl-4-(2-oxo-2-phenylethyl)-2-phenyl-1,2,3,4-tetrahydroquinoline-3-carboxamide
Synonyms: (2R,3R,4S)-N-benzyl-4-(2-oxo-2-phenylethyl)-2-phenyl-1,2,3,4-tetrahydroquinoline-3-carboxamide
CAS NO:1454837-46-7
Molecular Formula:
Molecular Weight: 460.576
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: (2R,3R,4S)-N-benzyl-4-(2-oxo-2-phenylethyl)-2-phenyl-1,2,3,4-tetrahydroquinoline-3-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4S)-N-benzyl-4-(2-oxo-2-phenylethyl)-2-phenyl-1,2,3,4-tetrahydroquinoline-3-carboxamide(1454837-46-7)
EPA Substance Registry System: (2R,3R,4S)-N-benzyl-4-(2-oxo-2-phenylethyl)-2-phenyl-1,2,3,4-tetrahydroquinoline-3-carboxamide(1454837-46-7)

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: 1454837-46-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1454837-46-7 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 1454837-46:
(9*1)+(8*4)+(7*5)+(6*4)+(5*8)+(4*3)+(3*7)+(2*4)+(1*6)=187
187 % 10 = 7
So 1454837-46-7 is a valid CAS Registry Number.

1454837-46-7Upstream product

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1454837-46-7Relevant 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

, 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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