Cas 1243378-70-2,2,6-di-tert-butyl-4-[(2-chloro-4-methylphenyl)aminocarbonyloxyimino]cyclohexa-2,5-dien-1-one

1243378-70-2

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Basic information

Product Name: 2,6-di-tert-butyl-4-[(2-chloro-4-methylphenyl)aminocarbonyloxyimino]cyclohexa-2,5-dien-1-one
Synonyms:
CAS NO:1243378-70-2
Molecular Formula:
Molecular Weight: 402.921
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: 2,6-di-tert-butyl-4-[(2-chloro-4-methylphenyl)aminocarbonyloxyimino]cyclohexa-2,5-dien-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 2,6-di-tert-butyl-4-[(2-chloro-4-methylphenyl)aminocarbonyloxyimino]cyclohexa-2,5-dien-1-one(1243378-70-2)
EPA Substance Registry System: 2,6-di-tert-butyl-4-[(2-chloro-4-methylphenyl)aminocarbonyloxyimino]cyclohexa-2,5-dien-1-one(1243378-70-2)

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: 1243378-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1243378-70-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,3,7 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1243378-70:
(9*1)+(8*2)+(7*4)+(6*3)+(5*3)+(4*7)+(3*8)+(2*7)+(1*0)=152
152 % 10 = 2
So 1243378-70-2 is a valid CAS Registry Number.

1243378-70-2Upstream product

1243378-12-2 2,6-di-tert-butyl-4-[(4-methylphenyl)aminocarbonyloxyimino]cyclohexa-2,5-dien-1-one

1243378-70-2Downstream Products

1243378-70-2Relevant academic research and scientific papers

Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime esrers: XI. Synthesis and halogenation of 4-[aryl(alkyl)aminocarbonyl-oxyimino] cyclohexa-2,5-dien-1-ones

Avdeenko,Konovalova,Sergeeva

experimental part, p. 830 - 843 (2010/10/21)

4-[Aryl(alkyl)aminocarbonyloxyimino]cyclohexa-2,5-dien-1-ones were synthesized by treatment of various substituted p-quinone monooximes with aryl isocyanates. The selectivity in the halogenation of the obtained p-quinone monooxime esters depended on the s

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