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75080-51-2

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75080-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75080-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,8 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75080-51:
(7*7)+(6*5)+(5*0)+(4*8)+(3*0)+(2*5)+(1*1)=122
122 % 10 = 2
So 75080-51-2 is a valid CAS Registry Number.

75080-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name spiro[1,3-benzodioxole-2,1'-cyclohexane]-5,6-dione

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:75080-51-2 SDS

75080-51-2Relevant articles and documents

Oxidations with Lead Tetraacetate. II. Oxidations of 2,2-Disubstituted 1,3-Benzodioxoles

Cole, Edward R.,Crank, George,Minh, H. T. Hai

, p. 527 - 543 (2007/10/02)

The oxidation of 2,2-disubstituted 1,3-benzodioxoles by lead tetraacetate proceeds readily to give 5-acetoxy and 5,6-dione derivatives as main products. 5,6-Diacetoxy compuonds and 5-carboxy derivatives are found in some instances as minor products.Oxidation of benzodioxoles substituted at the 5 and 6 positions with methoxyl groups or with a second dioxole ring results in oxidative loss of the dioxole ring.Relative effects of these substitutions on reactivity have been evaluated.The mechanism of ο-quinone formation is discussed and is postulated to occur via a tetraacetoxy intermediate.The 5-acetoxy derivatives and the ο-quinones, by hydrolysis and reduction respectively, serve as sources of 5-hydroxy and 5,6-dihydroxy benzodioxoles.

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