Cas 848933-32-4,5,7-bis-(<i>tert</i>-butyl-dimethyl-silanyloxy)-2-[4-(<i>tert</i>-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-benzo[1,4]oxathiine

848933-32-4

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Basic information

Product Name: 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-benzo[1,4]oxathiine
Synonyms: 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-benzo[1,4]oxathiine
CAS NO:848933-32-4
Molecular Formula:
Molecular Weight: 619.101
EINECS: N/A
Product Categories: N/A
Mol File: 848933-32-4.mol
Article Data: 1

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: 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-benzo[1,4]oxathiine(CAS DataBase Reference)
NIST Chemistry Reference: 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-benzo[1,4]oxathiine(848933-32-4)
EPA Substance Registry System: 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-benzo[1,4]oxathiine(848933-32-4)

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: 848933-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 848933-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,9,3 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 848933-32:
(8*8)+(7*4)+(6*8)+(5*9)+(4*3)+(3*3)+(2*3)+(1*2)=214
214 % 10 = 4
So 848933-32-4 is a valid CAS Registry Number.

848933-32-4Upstream product

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848933-32-4Relevant articles and documents

Easy synthesis of polyphenolic 4-thiaflavans with a 'double-faced' antioxidant activity

Capozzi,Lo Nostro,Menichetti,Nativi,Sarri

, p. 551 - 552 (2001)

Inverse electron demanding Diels-Alder reactions of o-thioquinones with styrenes, followed by simple manipulations of the obtained cycloadducts, allowed the synthesis of polyphenolic 4-thiaflavans which showed antioxidant activity miming either flavonoid

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