Cas 1370231-48-3,2-chloro-3-(3-methyl-4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-dione

1370231-48-3

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Basic information

Product Name: 2-chloro-3-(3-methyl-4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-dione
Synonyms: 2-chloro-3-(3-methyl-4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-dione
CAS NO:1370231-48-3
Molecular Formula:
Molecular Weight: 311.724
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: 2-chloro-3-(3-methyl-4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-chloro-3-(3-methyl-4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-dione(1370231-48-3)
EPA Substance Registry System: 2-chloro-3-(3-methyl-4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-dione(1370231-48-3)

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: 1370231-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1370231-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,2,3 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1370231-48:
(9*1)+(8*3)+(7*7)+(6*0)+(5*2)+(4*3)+(3*1)+(2*4)+(1*8)=123
123 % 10 = 3
So 1370231-48-3 is a valid CAS Registry Number.

1370231-48-3Upstream product

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1370231-48-3Relevant academic research and scientific papers

Reactions of 2-(4-hydroxyanilino)-1,4-naphthoquinones with cerium ammonium nitrate and pyridinium chlorochromate

Devyashina,Gornostaev,Gatilov

, p. 234 - 240 (2012/06/01)

Reactions of 2-(4-hydroxyarylamino)-1,4-naphthoquinones with cerium ammonium nitrate or pyridinium chlorochromate depending on the structure of initial substrate and the type of reagent led to the formation of 2-chloro-3-(4-cyclohexa-2,5-dienylideneamino)

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