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1-Cyclohexene-1-carboxylic acid, butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61574-65-0

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61574-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61574-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,7 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61574-65:
(7*6)+(6*1)+(5*5)+(4*7)+(3*4)+(2*6)+(1*5)=130
130 % 10 = 0
So 61574-65-0 is a valid CAS Registry Number.

61574-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohex-1-enecarboxylic acid butyl ester

1.2 Other means of identification

Product number -
Other names Butylester der Cyclohexen-(1)-carbonsaeure-(1)

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:61574-65-0 SDS

61574-65-0Downstream Products

61574-65-0Relevant academic research and scientific papers

Pd-Catalyzed Carbonylation of Vinyl Triflates to Afford α,β-Unsaturated Aldehydes, Esters, and Amides under Mild Conditions

Zhang, Shaoke,Neumann, Helfried,Beller, Matthias

, p. 3528 - 3532 (2019/05/24)

An efficient and general protocol for the synthesis of α,β-unsaturated aldehydes, esters, and amides via carbonylation of vinyl triflates including derivatives of camphor, ketoisophorone, verbenone, and pulegone was developed. Crucial for these transformations is the use of a specific palladium catalyst containing a pyridyl-substituted dtbpx-type ligand. This procedure also allows for an easy access of dicarbonylated products from the corresponding ketones.

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