Cas 1164469-52-6,2-[(Z)-(4-METHYLPHENYL)METHYLIDENE]-4,9-DIHYDRO-1H-CARBAZOL-1(3H)-ONE

1164469-52-6

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Basic information

Product Name: 2-[(Z)-(4-METHYLPHENYL)METHYLIDENE]-4,9-DIHYDRO-1H-CARBAZOL-1(3H)-ONE
Synonyms: 2-[(Z)-(4-METHYLPHENYL)METHYLIDENE]-4,9-DIHYDRO-1H-CARBAZOL-1(3H)-ONE
CAS NO:1164469-52-6
Molecular Formula: C20H17NO
Molecular Weight: 287.36
EINECS: N/A
Product Categories: N/A
Mol File: 1164469-52-6.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: 512.9±50.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.253±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 15.22±0.20(Predicted)
CAS DataBase Reference: 2-[(Z)-(4-METHYLPHENYL)METHYLIDENE]-4,9-DIHYDRO-1H-CARBAZOL-1(3H)-ONE(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(Z)-(4-METHYLPHENYL)METHYLIDENE]-4,9-DIHYDRO-1H-CARBAZOL-1(3H)-ONE(1164469-52-6)
EPA Substance Registry System: 2-[(Z)-(4-METHYLPHENYL)METHYLIDENE]-4,9-DIHYDRO-1H-CARBAZOL-1(3H)-ONE(1164469-52-6)

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: 1164469-52-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1164469-52-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,4,4,6 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1164469-52:
(9*1)+(8*1)+(7*6)+(6*4)+(5*4)+(4*6)+(3*9)+(2*5)+(1*2)=166
166 % 10 = 6
So 1164469-52-6 is a valid CAS Registry Number.

1164469-52-6Upstream product

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1164469-52-6Relevant articles and documents

Regioselective synthesis and antimicrobial screening of novel ketocarbazolodispiropyrrolidine derivatives

Periyasami, Govindasami,Raghunathan, Raghavachary,Surendiran, Gangadharan,Mathivanan, Narayanasamy

scheme or table, p. 959 - 966 (2009/09/29)

A series of novel dispiropyrrolidine derivatives have been synthesized through 1,3-dipolar cycloaddition reaction of azomethine ylide generated from sarcosin and di/tri ketone with the dipolarophile (E)-2-arylidine-1-keto-carbazoles. The cycloadducts keto

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