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Ethyl 3-hydroxy-4,4,4-trifluorobutyrate is a chemical compound characterized by its molecular formula C6H9F3O3. It is a colorless liquid with a distinctive fruity odor, known for its stability under normal conditions, although it can react with strong oxidizing agents. Ethyl 3-hydroxy-4,4,4-trifluorobutyrate is recognized for its applications in various industries, including the food and beverage sector, pharmaceutical production, and as an intermediate in organic synthesis.

99437-70-4

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99437-70-4 Usage

Uses

Used in Flavoring Agents:
Ethyl 3-hydroxy-4,4,4-trifluorobutyrate is utilized as a flavoring agent in the food and beverage industry, adding a fruity aroma and taste to various products.
Used in Pharmaceutical Production:
In the pharmaceutical sector, Ethyl 3-hydroxy-4,4,4-trifluorobutyrate serves as a key component in the manufacturing process of certain medications, contributing to their formulation and efficacy.
Used as an Intermediate in Organic Synthesis:
Ethyl 3-hydroxy-4,4,4-trifluorobutyrate is employed as an intermediate in organic synthesis, playing a crucial role in the synthesis of other complex organic compounds.
Used in Chemical Research:
Ethyl 3-hydroxy-4,4,4-trifluorobutyrate is also used in chemical research for studying the properties and reactions of trifluoromethyl-containing compounds, which can lead to advancements in the development of new materials and pharmaceuticals.
Safety Precautions:
Given its classification as a hazardous substance, Ethyl 3-hydroxy-4,4,4-trifluorobutyrate requires careful handling and storage to ensure safety in the workplace and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 99437-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,3 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99437-70:
(7*9)+(6*9)+(5*4)+(4*3)+(3*7)+(2*7)+(1*0)=184
184 % 10 = 4
So 99437-70-4 is a valid CAS Registry Number.

99437-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl (3S)-4,4,4-trifluoro-3-hydroxybutanoate

1.2 Other means of identification

Product number -
Other names (S)-(-)-ethyl 4,4,4-trifluoro-3-hydroxybutanoate

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:99437-70-4 SDS

99437-70-4Downstream Products

99437-70-4Relevant academic research and scientific papers

Novel unusual microbial dehalogenation during enantioselective reduction of ethyl 4,4,4-trifluoro acetoacetate with baker's yeast

Bertau, Martin

, p. 1267 - 1268 (2007/10/03)

In the course of investigating microbial syntheses for chiral pharmaceutical intermediates, ethyl 4,4,4-trifluoro acetoacetate (1) was submitted to baker's yeast reduction. With the purpose of obtaining the D-carbinol in high enantiopurity, several additives were tested for L-reductase inhibitor activity. Allyl alcohol proved to be not only a suitable additive, but also an inducer for effective defluorination of the substrate.

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