Cas 112825-65-7,1,4-Benzodioxin, 2,3-dichloro-5,7-bis(1,1-dimethylethyl)-2,3-dihydro-

112825-65-7

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Basic information

Product Name: 1,4-Benzodioxin, 2,3-dichloro-5,7-bis(1,1-dimethylethyl)-2,3-dihydro-
Synonyms:
CAS NO:112825-65-7
Molecular Formula: C16H22Cl2O2
Molecular Weight: 317.255
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: 1,4-Benzodioxin, 2,3-dichloro-5,7-bis(1,1-dimethylethyl)-2,3-dihydro-(CAS DataBase Reference)
NIST Chemistry Reference: 1,4-Benzodioxin, 2,3-dichloro-5,7-bis(1,1-dimethylethyl)-2,3-dihydro-(112825-65-7)
EPA Substance Registry System: 1,4-Benzodioxin, 2,3-dichloro-5,7-bis(1,1-dimethylethyl)-2,3-dihydro-(112825-65-7)

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: 112825-65-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112825-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,2 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112825-65:
(8*1)+(7*1)+(6*2)+(5*8)+(4*2)+(3*5)+(2*6)+(1*5)=107
107 % 10 = 7
So 112825-65-7 is a valid CAS Registry Number.

112825-65-7Upstream product

110307-00-1 5,7-di-tert-butyl-1,4-benzodioxin

112825-65-7Downstream Products

112825-65-7Relevant academic research and scientific papers

Synthesis of 1,2-Benzoquinones by the Oxidation of 1,4-Benzodioxins by Peroxide Derivatives

Kashima, Choji,Tomotake, Atsushi,Omote, Yoshimori

, p. 785 - 788 (2007/10/02)

The oxidation reaction of 1,4-benzodioxin 1 by m-chloroperbenzoic acid (m-CPBA) and t-butyl hydroperoxide (t-BHP) are reported. 1,2-Benzoquinone 2 was given in moderate yields by the m-CPBA oxidation of 1,4-benzodioxin 1, while 1,2-benzoquinone 2 was predominantly formed by t-BHP oxidation.

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