Cas 39876-28-3,6-HYDROXY-5-PHENYL-1,2-DIHYDRO-4H-PYRROLO[3,2,1-IJ]QUINOLIN-4-ONE

39876-28-3

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Basic information

Product Name: 6-HYDROXY-5-PHENYL-1,2-DIHYDRO-4H-PYRROLO[3,2,1-IJ]QUINOLIN-4-ONE
Synonyms: TOSLAB 798066;6-HYDROXY-5-PHENYL-1,2-DIHYDRO-4H-PYRROLO[3,2,1-IJ]QUINOLIN-4-ONE;BUTTPARK 135\40-42;AURORA KA-3685
CAS NO:39876-28-3
Molecular Formula: C₁₇H₁₃NO₂
Molecular Weight: 263.29
EINECS: N/A
Product Categories: N/A
Mol File: 39876-28-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 452.1°C at 760 mmHg
Flash Point: 227.2°C
Appearance: /
Density: 1.4g/cm³
Vapor Pressure: 5.82E-09mmHg at 25°C
Refractive Index: 1.736
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6-HYDROXY-5-PHENYL-1,2-DIHYDRO-4H-PYRROLO[3,2,1-IJ]QUINOLIN-4-ONE(CAS DataBase Reference)
NIST Chemistry Reference: 6-HYDROXY-5-PHENYL-1,2-DIHYDRO-4H-PYRROLO[3,2,1-IJ]QUINOLIN-4-ONE(39876-28-3)
EPA Substance Registry System: 6-HYDROXY-5-PHENYL-1,2-DIHYDRO-4H-PYRROLO[3,2,1-IJ]QUINOLIN-4-ONE(39876-28-3)

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: 39876-28-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 39876-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,7 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39876-28:
(7*3)+(6*9)+(5*8)+(4*7)+(3*6)+(2*2)+(1*8)=173
173 % 10 = 3
So 39876-28-3 is a valid CAS Registry Number.

InChI:InChI=1/C17H13NO2/c19-16-13-8-4-7-12-9-10-18(15(12)13)17(20)14(16)11-5-2-1-3-6-11/h1-8,20H,9-10H2

39876-28-3Upstream product

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39876-28-3Relevant academic research and scientific papers

Palladium-catalyzed double C-H functionalization of 2-aryl-1,3-dicarbonyl compounds: A facile access to alkenylated benzopyrans

Choppakatla, Subrahmanyam,Dachepally, Aravind Kumar,Bollikolla, Hari Babu

, p. 2488 - 2491 (2016)

The present study reports the development of a palladium-catalyzed oxidative annulation/nucleophilic substitution sequence affording a library of alkenylated benzopyrans using 2-aryl-1,3-dicarbonyl compounds and allylic acetate. The process is compatible

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