Cas 155694-76-1,1-N-acetyl-4-keto-6-methoxy-2-phenyl-3-(phenylseleno)-1,2,3,4-tetrahydroquinoline

155694-76-1

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Basic information

Product Name: 1-N-acetyl-4-keto-6-methoxy-2-phenyl-3-(phenylseleno)-1,2,3,4-tetrahydroquinoline
Synonyms: 1-N-acetyl-4-keto-6-methoxy-2-phenyl-3-(phenylseleno)-1,2,3,4-tetrahydroquinoline
CAS NO:155694-76-1
Molecular Formula:
Molecular Weight: 450.396
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: 1-N-acetyl-4-keto-6-methoxy-2-phenyl-3-(phenylseleno)-1,2,3,4-tetrahydroquinoline(CAS DataBase Reference)
NIST Chemistry Reference: 1-N-acetyl-4-keto-6-methoxy-2-phenyl-3-(phenylseleno)-1,2,3,4-tetrahydroquinoline(155694-76-1)
EPA Substance Registry System: 1-N-acetyl-4-keto-6-methoxy-2-phenyl-3-(phenylseleno)-1,2,3,4-tetrahydroquinoline(155694-76-1)

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: 155694-76-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155694-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,9 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155694-76:
(8*1)+(7*5)+(6*5)+(5*6)+(4*9)+(3*4)+(2*7)+(1*6)=171
171 % 10 = 1
So 155694-76-1 is a valid CAS Registry Number.

155694-76-1Upstream product

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155694-76-1Relevant academic research and scientific papers

Synthesis of Isocoumarin, 1-Isoquinolone and 4(1H)-Quinolone Derivatives via Seleno-intermediates

Izumi, Taeko,Morishita, Nobuya

, p. 145 - 152 (2007/10/02)

The reaction of 2-styrylbenzoic acid 2 with N-phenylselenosuccinimide (N-PPS) affords 3-phenyl-iso-coumarin derivatives 3 and 3,4-dihydro-3-phenyl-4-(phenylseleno)isocoumarins 4 via selenolactonization.The reaction of 2-styrylbenzamides 5 and 1-(2-aminoph

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