Cas 86604-24-2,Benzenesulfonamide, N-[3,5-bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-

86604-24-2

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Basic information

Product Name: Benzenesulfonamide, N-[3,5-bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-
Synonyms:
CAS NO:86604-24-2
Molecular Formula: C20H25NO3S
Molecular Weight: 359.489
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: Benzenesulfonamide, N-[3,5-bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N-[3,5-bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-(86604-24-2)
EPA Substance Registry System: Benzenesulfonamide, N-[3,5-bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-(86604-24-2)

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: 86604-24-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86604-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,0 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86604-24:
(7*8)+(6*6)+(5*6)+(4*0)+(3*4)+(2*2)+(1*4)=142
142 % 10 = 2
So 86604-24-2 is a valid CAS Registry Number.

86604-24-2Upstream product

61551-45-9 4-phenylsulfonylamino-2,6-di-tert-butylphenol

86604-24-2Downstream Products

1131615-19-4 (Z)-N-(3,5-di-tert-butyl-5,6,6-trichloro-4-oxocyclohex-2-en-1-ylidene)benzenesulfonamide

86604-24-2Relevant academic research and scientific papers

DEGENERATE Z,E ISOMERIZATION OF 4-ARYLSULFONYLIMINO-2,6-DI-TERT-BUTYL-1,4-BENZOQUINONES

Belov, V. V.,Loban', S. V.,Burmistrov, K. S.,Prosyanik, A. V.

, p. 730 - 732 (2007/10/02)

The kinetic parameters of the degenerate Z,E isomerization of 4-arylsulfonylimino-2,6-di-tert-butyl-1,4-benzoquinones in tetrachloroethylene were studied by the dynamic PMR method.An inversion mechanism for the process was established on the basis of a co

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