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13035-03-5

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13035-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13035-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,3 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13035-03:
(7*1)+(6*3)+(5*0)+(4*3)+(3*5)+(2*0)+(1*3)=55
55 % 10 = 5
So 13035-03-5 is a valid CAS Registry Number.

13035-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroperoxy-1-(1-hydroperoxy-4-methylcyclohexyl)peroxy-4-methylcyclohexane

1.2 Other means of identification

Product number -
Other names Bis-<1-hydroperoxy-4-methyl-cyclohexyl>-peroxid

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:13035-03-5 SDS

13035-03-5Upstream product

13035-03-5Downstream Products

13035-03-5Relevant articles and documents

Synthesis of cyclic peroxides containing the Si-gem-bisperoxide fragment. 1,2,4,5,7,8-hexaoxa-3-silonanes as a new class of peroxides

Terent'ev, Alexander O.,Platonov, Maxim M.,Tursina, Anna I.,Chernyshev, Vladimir V.,Nikishin, Gennady I.

, p. 3169 - 3174 (2008/09/19)

(Chemical Equation Presented) A method was developed for the synthesis of the previously unknown class of organic peroxides, 1,2,4,5,7,8-hexaoxa-3- silonanes, based on the reaction of dialkyldichlorosilanes with 1,1′-dihydroperoxyperoxides. 1,2,4,5,7,8-Hexaoxa-3-silonanes are rather stable under ambient conditions and were characterized by NMR spectroscopy, X-ray diffraction, and elemental analysis. Their yields are in a range of 59-96%. The attempts were made to prepare 1,2,4,5-tetraoxa-3-silinanes by the reaction of dialkyldichlorosilanes with gem-bishydroperoxides. 1,2,4,5-Tetraoxa-3-silinanes were detected by NMR spectroscopy; these compounds rapidly decompose upon isolation.

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