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85981-67-5

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85981-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85981-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,8 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85981-67:
(7*8)+(6*5)+(5*9)+(4*8)+(3*1)+(2*6)+(1*7)=185
185 % 10 = 5
So 85981-67-5 is a valid CAS Registry Number.

85981-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyl-5-(4-nitrophenyl)dioxolane

1.2 Other means of identification

Product number -
Other names 1,2-Dioxolane,3,3-dimethyl-5-(4-nitrophenyl)

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:85981-67-5 SDS

85981-67-5Downstream Products

85981-67-5Relevant articles and documents

Organic Peroxides, XXIV. - On the Barton Type Cyclization of Organic Hydroperoxides

Kropf, Heinz,Wallis, Helmut von

, p. 610 - 623 (2007/10/02)

On the earlier reported cyclization conditions the hydroperoxides 1e-g yield the 1,2-dioxolanes 2e-g, but the hydroperoxide 1d gives the 1,2-dioxocane 2d only in low yield.On the reaction of the hydroperoxides 1a and 1b as examples for the reported cyclization reactions the compounds obtained besides the cyclization products are ascertained particularly (symmetric and unsymmetric dialkyl peroxides 4 and 7, alcohols 3, carbonyl compounds 5 and 6).The hydroperoxides 1h and 1i yield the symmetric and unsymmetric dialkyl peroxides as peroxidic compounds only.The hydrocarbons 10a and 10b as well as the alcohols 3a and 3b do not react on the cyclization conditions. - Reaction of 1a with lead(IV) acetate in acetic acid yields the alkyl methyl peroxide 9a, in propionic acid/n-pentane the alkyl ethyl peroxide 9b. - Cer(IV) sulfate reacts as cyclodehydrogenation reagent also. - The earlier postulated Barton type mechanism was made certain on the reasons of the results.

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