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1,2-Dioxetane-3-methanol, 4,4-dimethyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

403731-45-3

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403731-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403731-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,7,3 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 403731-45:
(8*4)+(7*0)+(6*3)+(5*7)+(4*3)+(3*1)+(2*4)+(1*5)=113
113 % 10 = 3
So 403731-45-3 is a valid CAS Registry Number.

403731-45-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyl-4-hydroxymethyl-4-phenyl-1,2-dioxetane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:403731-45-3 SDS

403731-45-3Relevant academic research and scientific papers

Spiroiminodihydantoin is a major product in the photooxidation of 2′-deoxyguanosine by the triplet states and oxyl radicals generated from hydroxyacetophenone photolysis and dioxetane thermolysis

Adam, Waldemar,Arnold, Markus A.,Gruene, Matthias,Nau, Werner M.,Pischel, Uwe,Saha-Moeller, Chantu R.

, p. 537 - 540 (2007/10/03)

(formula presented) Photolysis of hydroxyacetophenone and thermolysis of the corresponding dioxetane afford spiroiminodihydantoin rather than 4,8-dihydro-4-hydroxy-8-oxo-2′-deoxyguanosine (4-HO-8-oxodG) through the oxidation of 2′-deoxyguanosine (dG) by triplet-excited hydroxyacetophenone and the peroxyl radicals derived thereof by α cleavage and subsequent oxygen trapping. The structure of the spiroiminodihydantoin is assigned by the SELINQUATE NMR technique, which unequivocally establishes the spirocyclic connectivity.

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