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488711-09-7

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488711-09-7 Usage

General Description

The chemical "Butanoic acid, 4,4,4-trifluoro-3-oxo-, methyl ester, radical ion(1+) (9CI)" is a compound consisting of butanoic acid with a 4,4,4-trifluoro-3-oxo- group and a methyl ester. It also contains a radical ion with a positive charge. Butanoic acid, 4,4,4-trifluoro-3-oxo-, methyl ester, radical ion(1+) (9CI) is likely to have properties and reactivity characteristic of both butanoic acid and the 4,4,4-trifluoro-3-oxo- group, as well as the reactivity associated with radical ions. Its specific use and potential effects would depend on its intended application and the environment in which it is used.

Check Digit Verification of cas no

The CAS Registry Mumber 488711-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,7,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 488711-09:
(8*4)+(7*8)+(6*8)+(5*7)+(4*1)+(3*1)+(2*0)+(1*9)=187
187 % 10 = 7
So 488711-09-7 is a valid CAS Registry Number.

488711-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4,4,4-trifluoro-3-oxobutanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid,4,4,4-trifluoro-3-oxo-,methyl ester

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:488711-09-7 SDS

488711-09-7Relevant articles and documents

Electrochemical synthesis of versatile ammonium oxides under metal catalyst-, exogenous-oxidant-, and exogenous-electrolyte-free conditions

Yuan, Yong,Li, Liang-Sen,Zhang, Lin,Wang, Feng,Jiang, Lin,Zuo, Lin,Wang, Qi,Hu, Jian-Guo,Lei, Aiwen

supporting information, p. 2768 - 2771 (2021/03/23)

An electrochemical oxidative cross-coupling reaction between 2.5-substituted-pyrazolin-5-ones and ammonium thiocyanate has been developed, which resulted in a series of unprecedented cross-coupling products under metal catalyst-, exogenous-oxidant-, and exogenous-electrolyte-free conditions. It is worth noting that since the resulting cross-coupling products are nearly insoluble in MeCN, the pure product could be afforded without silica gel column purification. In addition, the prepared ammonium oxides are versatile building blocks for synthesizing functionalized pyrazole derivatives.

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