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83643-84-9

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83643-84-9 Usage

Description

METHYL 4,4,4-TRIFLUOROACETOACETATE is an organic compound that serves as a versatile intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is characterized by its trifluoromethyl group, which imparts unique properties to the molecule, making it a valuable building block in organic chemistry.

Uses

Used in Pharmaceutical Industry:
METHYL 4,4,4-TRIFLUOROACETOACETATE is used as a drug intermediate for the synthesis of various pharmaceuticals. Its unique trifluoromethyl group allows for the development of new and innovative drugs with improved pharmacological properties.
Used in Agrochemical Industry:
METHYL 4,4,4-TRIFLUOROACETOACETATE is also used as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its reactivity and stability make it a valuable component in the development of effective and environmentally friendly agricultural products.
Used as a Cyclization Catalyst:
METHYL 4,4,4-TRIFLUOROACETOACETATE is used as a cyclization catalyst in organic synthesis. Its ability to promote the formation of cyclic compounds can be utilized in the synthesis of complex organic molecules, including natural products and pharmaceuticals.
Used as an Oxidation Catalyst:
METHYL 4,4,4-TRIFLUOROACETOACETATE can also function as an oxidation catalyst, facilitating the conversion of alcohols to aldehydes or ketones. This property is useful in the synthesis of various organic compounds and can be applied in various industries, including pharmaceuticals and agrochemicals.
Used as a Halogenation Catalyst:
Furthermore, METHYL 4,4,4-TRIFLUOROACETOACETATE can act as a halogenation catalyst, enabling the introduction of halogen atoms into organic molecules. This can be particularly useful in the synthesis of halogenated compounds, which have applications in various fields, such as pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 83643-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,4 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83643-84:
(7*8)+(6*3)+(5*6)+(4*4)+(3*3)+(2*8)+(1*4)=149
149 % 10 = 9
So 83643-84-9 is a valid CAS Registry Number.

83643-84-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • TCI America

  • (T1245)  Methyl 4,4,4-Trifluoroacetoacetate  >96.0%(GC)

  • 83643-84-9

  • 5g

  • 590.00CNY

  • Detail
  • TCI America

  • (T1245)  Methyl 4,4,4-Trifluoroacetoacetate  >96.0%(GC)

  • 83643-84-9

  • 25g

  • 1,770.00CNY

  • Detail
  • Alfa Aesar

  • (L10140)  Methyl 4,4,4-trifluoroacetoacetate, 95%   

  • 83643-84-9

  • 5g

  • 580.0CNY

  • Detail
  • Alfa Aesar

  • (L10140)  Methyl 4,4,4-trifluoroacetoacetate, 95%   

  • 83643-84-9

  • 25g

  • 2135.0CNY

  • Detail

83643-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4,4,4-Trifluoroacetoacetate

1.2 Other means of identification

Product number -
Other names METHYL 4,4,4-TRIFLUOROACETOACETATE

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:83643-84-9 SDS

83643-84-9Relevant 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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