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1,3-Dioxolane, 4-methyl-2,2-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77130-19-9

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77130-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77130-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,3 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77130-19:
(7*7)+(6*7)+(5*1)+(4*3)+(3*0)+(2*1)+(1*9)=119
119 % 10 = 9
So 77130-19-9 is a valid CAS Registry Number.

77130-19-9SDS

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 4-methyl-2,2-diphenyl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane,4-methyl-2,2-diphenyl

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:77130-19-9 SDS

77130-19-9Downstream Products

77130-19-9Relevant academic research and scientific papers

Highly efficient heterogeneous acetalization of carbonyl compounds catalyzed by a titanium cation-exchanged montmorillonite

Kawabata, Tomonori,Mizugaki, Tomoo,Ebitani, Kohki,Kaneda, Kiyotomi

, p. 8329 - 8332 (2007/10/03)

The titanium cation-exchanged montmorillonite efficiently catalyzed the selective acetalization of various carbonyl compounds as a recyclable solid acid. This heterogeneous catalyst has an advantage of a strikingly simple workup procedure over conventional homogeneous acids.

FACILE SYNTHETIC METHODS OF ACETALS AND CROWN ETHERS FROM THE REACTION OF DIPHENYLDIAZOMETHANE WITH 2,3-DICHLORO-5,6-DICYANOBENZOQUINONE IN THE PRESENCE OF ALCOHOLS

Oshima, Takumi,Nishioka, Ryoji,Nagai, Toshikazu

, p. 3919 - 3922 (2007/10/02)

The reaction of diphenyldiazomethane with 2,3-dichloro-5,6-dicyanobenzoquinone in the presence of alcohols and thiols gave the corresponding benzophenone acetals and thioacetals at 20-25 deg C in 1,2-dichloroethane.The mechanism of the reaction will be discussed.

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