Cas 75498-75-8,2,6-Di-tert-butyl-4-[hydroperoxy-(4-methoxy-phenyl)-methylimino]-cyclohexa-2,5-dienone

75498-75-8

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Basic information

Product Name: 2,6-Di-tert-butyl-4-[hydroperoxy-(4-methoxy-phenyl)-methylimino]-cyclohexa-2,5-dienone
Synonyms: 2,6-Di-tert-butyl-4-[hydroperoxy-(4-methoxy-phenyl)-methylimino]-cyclohexa-2,5-dienone
CAS NO:75498-75-8
Molecular Formula:
Molecular Weight: 371.477
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-[hydroperoxy-(4-methoxy-phenyl)-methylimino]-cyclohexa-2,5-dienone(CAS DataBase Reference)
NIST Chemistry Reference: 2,6-Di-tert-butyl-4-[hydroperoxy-(4-methoxy-phenyl)-methylimino]-cyclohexa-2,5-dienone(75498-75-8)
EPA Substance Registry System: 2,6-Di-tert-butyl-4-[hydroperoxy-(4-methoxy-phenyl)-methylimino]-cyclohexa-2,5-dienone(75498-75-8)

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: 75498-75-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75498-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,9 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75498-75:
(7*7)+(6*5)+(5*4)+(4*9)+(3*8)+(2*7)+(1*5)=178
178 % 10 = 8
So 75498-75-8 is a valid CAS Registry Number.

75498-75-8Upstream product

54034-15-0 (C₆H₄(OCH₃)HCNC₆H₂(C₄H₉)2OH)

75498-75-8Downstream Products

75498-75-8Relevant academic research and scientific papers

NEW 1,1-AMINO HYDROPEROXIDES FROM REGIOSELECTIVE OXYGENATION OF 4-(N-ARYLMETHYLENEAMINO)-2,6-DI-t-BUTYLPHENOLS.

Nishinaga, A.,Shimizu, T.,Matsuura, T.

, p. 1265 - 1268 (2007/10/02)

The oxygenation of 4-(N-arylmethyleneamino)-2,6-di-t-butylphenols with Co(Salpr), a five coordinate Co(II) Schiff base complex, in CH2Cl2 results in the regioselective hydroperoxylation at the imino carbon to give N-(1-aryl-1-hydroperoxymethyl)-3,5-di-t-butyl-p-benzoquinone monoimines, which give exclusively the corresponding amides and 2,6-di-t-butyl-p-benzoquinone in an aerobic solution of KOH in 90percent EtOH.

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