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propan-2-yl cyclohexylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60784-57-8

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60784-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60784-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,8 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60784-57:
(7*6)+(6*0)+(5*7)+(4*8)+(3*4)+(2*5)+(1*7)=138
138 % 10 = 8
So 60784-57-8 is a valid CAS Registry Number.

60784-57-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name propan-2-yl 2-cyclohexylacetate

1.2 Other means of identification

Product number -
Other names propan-2-yl cyclohexylacetate

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:60784-57-8 SDS

60784-57-8Downstream Products

60784-57-8Relevant academic research and scientific papers

Efficient microwave-assisted esterification reaction employing methanesulfonic acid supported on alumina as catalyst

Fabian, Lucas,Gomez, Matias,Kuran, Juan A. Caturelli,Moltrasio, Graciela,Moglioni, Albertina

, p. 2386 - 2392 (2014/07/22)

A rapid and efficient protocol assisted by microwave irradiation for the synthesis of esters using methanesulfonic acid (CH3SO3H) supported on Al2O3 (AMA) as catalyst and free of solvent is described. The products were obtained in good yields and purity, with reduced reaction time, and the process is simple and environmentally benign. Copyright

Improved Cs2CO3 promoted O-alkylation of acids

Parrish, Jay P.,Dueno, Eric E.,Kim, Seok-In,Jung, Kyung Woon

, p. 2687 - 2700 (2007/10/03)

Cesium carbonate mediated O-alkylation of carboxylic acids was efficiently carried out under mild in situ conditions to give the corresponding esters exclusively. Chiral templates including α-hydroxy and α-alkoxy acids were also converted to their corresponding esters with no observed racemization.

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