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ETHYL 3-BROMOPROPIONATE-2,2,3,3-D4 is a chemical compound that serves as an intriguing building block in the field of chemistry. It is characterized by its light yellow oil appearance and holds potential for various applications due to its unique chemical properties.

14341-55-0

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14341-55-0 Usage

Uses

Used in Chemical Synthesis:
ETHYL 3-BROMOPROPIONATE-2,2,3,3-D4 is used as a building block for the synthesis of various organic compounds. Its unique structure allows it to be a valuable component in the creation of different molecules, contributing to the development of new materials and substances.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL 3-BROMOPROPIONATE-2,2,3,3-D4 is used as an intermediate in the production of certain drugs. Its chemical properties make it suitable for the synthesis of specific medicinal compounds, potentially leading to the development of new treatments and therapies.
Used in Research and Development:
ETHYL 3-BROMOPROPIONATE-2,2,3,3-D4 is also utilized in research and development settings, where it can be employed to study chemical reactions and explore new pathways for synthesizing complex molecules. Its light yellow oil form and unique properties make it an interesting subject for scientific investigation.
Used in Material Science:
In the field of material science, ETHYL 3-BROMOPROPIONATE-2,2,3,3-D4 can be used as a component in the development of new materials with specific properties. Its chemical structure may contribute to the creation of materials with enhanced characteristics, such as improved stability or reactivity.
Overall, ETHYL 3-BROMOPROPIONATE-2,2,3,3-D4 is a versatile compound with a wide range of potential applications across various industries, including chemical synthesis, pharmaceuticals, research and development, and material science. Its unique properties and light yellow oil appearance make it an interesting building block for the creation of new compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 14341-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,4 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14341-55:
(7*1)+(6*4)+(5*3)+(4*4)+(3*1)+(2*5)+(1*5)=80
80 % 10 = 0
So 14341-55-0 is a valid CAS Registry Number.

14341-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl-3-bromopropionate-d4

1.2 Other means of identification

Product number -
Other names ethyl 3-bromo-2,2,3,3-tetradeuteriopropanoate

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:14341-55-0 SDS

14341-55-0Downstream Products

14341-55-0Relevant academic research and scientific papers

Quantitation of Nine Lactones in Dairy Cream by Stable Isotope Dilution Assays Based on Novel Syntheses of Carbon-13-Labeled γ-Lactones and Deuterium-Labeled δ-Lactones in Combination with Comprehensive Two-Dimensional Gas Chromatography with Time-of-Flight Mass Spectrometry

Schütt, Jessica,Schieberle, Peter

, p. 10534 - 10541 (2017)

Lactones are well-known aroma compounds in, e.g., fruits and fermented foods as well as in dairy products, such as cream or milk powders. The latter are often used in confectionary products, e.g., milk chocolate. Lactones are suggested to contribute to the distinct aroma of dairy products and have also been reported in milk chocolate. However, data on their contribution to the overall aroma of this type of chocolate are scarce. As a result of their pH-dependent instability and their low volatility, a reliable quantitation of lactones is a challenge. Thus, to allow for a quantitation of nine lactones in one single comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometry in electron ionization mode run, new synthetic routes were developed for five carbon-13-labeled γ-lactones and four deuterium-labeled δ-lactones, with the isotope label in the ring to be used in stable isotope dilution assays. The concentrations of the nine lactones were then analyzed in raw and pasteurized cream as well as in a heat-treated raw cream. δ-Dodecalactone and δ-decalactone showed the highest concentrations in both the raw and pasteurized cream. In the latter, δ-dodecalactone reached a 2.5-fold higher concentration compared to the raw cream. Subsequent heat treatments in a lab scale showed a further increase by factors of 13 and 19, respectively, suggesting a high potential of lactone precursors in cream. The results serve as a basis for further studies on lactone formation in other thermally processed products, such as milk chocolate.

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