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Hydroperoxide, cycloheptylidenebis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

352018-71-4

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352018-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352018-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,0,1 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 352018-71:
(8*3)+(7*5)+(6*2)+(5*0)+(4*1)+(3*8)+(2*7)+(1*1)=114
114 % 10 = 4
So 352018-71-4 is a valid CAS Registry Number.

352018-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cycloheptane-1,1-diyl dihydroperoxide

1.2 Other means of identification

Product number -
Other names cycloheptylidene-1,1-bishydroperoxide

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:352018-71-4 SDS

352018-71-4Upstream product

352018-71-4Relevant academic research and scientific papers

Reaction of enol ethers with the I2-H2O2 system: Synthesis of 2-iodo-1-methoxy hydroperoxides and their deperoxidation and demethoxylation to 2-iodo ketones

Terent'ev, Alexander O.,Borisov, Alexander M.,Platonov, Maxim M.,Starikova, Zoya A.,Chernyshev, Vladimir V.,Nikishin, Gennady I.

, p. 4159 - 4166 (2009)

The reaction of enol ethers with the I2-H2O 2 system in diethyl ether affords 2-iodo ketones and the previously unknown 2-iodo-1-methoxy hydroperoxides. In the presence of the I 2-H2O2 system, the latter compounds undergo deperoxidation and demethoxylation to form 2-iodo ketones. The reaction conditions were found for the synthesis of 2-iodo ketones from enol ethers in 67-94% yields. Georg Thieme Verlag Stuttgart - New York.

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