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64057-79-0

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64057-79-0 Usage

Uses

It is used as an intermediate in enantioselective tsuji enol silane allylation reaction.

Check Digit Verification of cas no

The CAS Registry Mumber 64057-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,5 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64057-79:
(7*6)+(6*4)+(5*0)+(4*5)+(3*7)+(2*7)+(1*9)=130
130 % 10 = 0
So 64057-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O3/c1-7(2)5-11-9(10)12-6-8(3)4/h1,3,5-6H2,2,4H3

64057-79-0 Well-known Company Product Price

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  • Alfa Aesar

  • (B20414)  Dimethallyl carbonate, 97%   

  • 64057-79-0

  • 5g

  • 415.0CNY

  • Detail
  • Alfa Aesar

  • (B20414)  Dimethallyl carbonate, 97%   

  • 64057-79-0

  • 25g

  • 1703.0CNY

  • Detail

64057-79-0SDS

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 Dimethallyl Carbonate

1.2 Other means of identification

Product number -
Other names bis(2-methylprop-2-enyl) carbonate

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:64057-79-0 SDS

64057-79-0Relevant articles and documents

Organic carbonate synthesis from CO2 and alcohol over CeO 2 with 2-cyanopyridine: Scope and mechanistic studies

Honda, Masayoshi,Tamura, Masazumi,Nakagawa, Yoshinao,Nakao, Kenji,Suzuki, Kimihito,Tomishige, Keiichi

, p. 95 - 107 (2014/09/17)

The combination system of CeO2-catalyzed carboxylation and 2-cyanopyridine hydration (CeO2 + 2-cyanopyridine system) is effective for the direct synthesis of organic carbonates from CO2 and alcohols. This catalyst system can be applied to various alcohols to afford the corresponding carbonates in high alcohol-based yields. The hydration of 2-cyanopyridine over CeO2 rapidly proceeds under the low concentration of water, which can remove the water from the reaction media. Since the reaction is limited by the chemical equilibrium, the removal of water remarkably shifts the chemical equilibrium to the carbonate side, leading to high carbonate yields. In addition, 2-picolinamide that is produced by hydration of 2-cyanopyridine forms an intramolecular hydrogen bonding between H atom of the amide group and N atom of the pyridine ring, which weakens the adsorption of 2-picolinamide on CeO2 by reduction of the acidity. The reaction mechanism of DMC formation in CeO2 + 2-cyanopyridine system is also proposed.

Synthesis of carbonates directly from 1 atm CO2 and alcohols using CH2Cl2

Yamazaki, Yusuke,Kakuma, Kasumi,Du, Ya,Saito, Susumu

experimental part, p. 9675 - 9680 (2011/02/24)

We introduced here a new one-pot, general procedure for the preparation of dialkyl carbonates from alcohols in a straightforward fashion under 1 atm pressure of CO2 using Cs2CO3 and CH 2Cl2 as key reagents.

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