Cas 98127-52-7,12-(2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-2,2-dimethyl-2,3-dihydro-1H-benzo[f]pyrido[1,2-a]indole-4,6,11-trione

98127-52-7

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Basic information

Product Name: 12-(2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-2,2-dimethyl-2,3-dihydro-1H-benzo[f]pyrido[1,2-a]indole-4,6,11-trione
Synonyms: 12-(2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-2,2-dimethyl-2,3-dihydro-1H-benzo[f]pyrido[1,2-a]indole-4,6,11-trione
CAS NO:98127-52-7
Molecular Formula:
Molecular Weight: 431.488
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: 12-(2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-2,2-dimethyl-2,3-dihydro-1H-benzo[f]pyrido[1,2-a]indole-4,6,11-trione(CAS DataBase Reference)
NIST Chemistry Reference: 12-(2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-2,2-dimethyl-2,3-dihydro-1H-benzo[f]pyrido[1,2-a]indole-4,6,11-trione(98127-52-7)
EPA Substance Registry System: 12-(2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-2,2-dimethyl-2,3-dihydro-1H-benzo[f]pyrido[1,2-a]indole-4,6,11-trione(98127-52-7)

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: 98127-52-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98127-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,2 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98127-52:
(7*9)+(6*8)+(5*1)+(4*2)+(3*7)+(2*5)+(1*2)=157
157 % 10 = 7
So 98127-52-7 is a valid CAS Registry Number.

98127-52-7Upstream product

126-81-8 dimedone

98127-52-7Downstream Products

98127-52-7Relevant academic research and scientific papers

A Novel Synthetic Route to Heterocyclic Quinones

Hamdan, Abdulla J.,Moore, Harold W.

, p. 3427 - 3428 (1985)

A new synthetic route to heterocyclic quinones is presented.This involves the addition of nucleophiles to the quinone methides generated from azidoquinones.The resulting azidohydroquinones proceed to aminoquinones which, in turn, lead to heterocyclic quin

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