Cas 1197024-76-2,7,7-dimethyl-2-(4-methylphenyl)-4-(4-β-D-allopyranosyloxyphenyl)-5-oxo-4,6,7,8-tetrahydroquinoline

1197024-76-2

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Basic information

Product Name: 7,7-dimethyl-2-(4-methylphenyl)-4-(4-β-D-allopyranosyloxyphenyl)-5-oxo-4,6,7,8-tetrahydroquinoline
Synonyms:
CAS NO:1197024-76-2
Molecular Formula:
Molecular Weight: 521.61
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: 7,7-dimethyl-2-(4-methylphenyl)-4-(4-β-D-allopyranosyloxyphenyl)-5-oxo-4,6,7,8-tetrahydroquinoline(CAS DataBase Reference)
NIST Chemistry Reference: 7,7-dimethyl-2-(4-methylphenyl)-4-(4-β-D-allopyranosyloxyphenyl)-5-oxo-4,6,7,8-tetrahydroquinoline(1197024-76-2)
EPA Substance Registry System: 7,7-dimethyl-2-(4-methylphenyl)-4-(4-β-D-allopyranosyloxyphenyl)-5-oxo-4,6,7,8-tetrahydroquinoline(1197024-76-2)

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: 1197024-76-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1197024-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,0,2 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1197024-76:
(9*1)+(8*1)+(7*9)+(6*7)+(5*0)+(4*2)+(3*4)+(2*7)+(1*6)=162
162 % 10 = 2
So 1197024-76-2 is a valid CAS Registry Number.

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1197024-76-2Relevant academic research and scientific papers

Synthesis of 2-aryl-4-(4-β-D-allopyranosyloxyphenyl)4,6,7,8- tetrahydroquinolin-5(1H)-one derivatives under solvent-free conditions and study of sedative activity

Yang, Congling,Lv, Shiming,Li, Ying,Yin, Shufan

, p. 910 - 914 (2011/05/06)

Under solvent-free conditions, syntheses of 2-aryl-4-(4-β-D- allopyranosyloxyphenyl)-4,6,7,8tetrahydroquinolin-5(1H)-one derivatives were carried out from chalcone (2a-2e), cyclohexane-1,3-dione (3), and NH 4OAc in excellent yield without using

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