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3-Oxo-2-propylheptanoic Acid Ethyl Ester, with the chemical formula C10H18O3 and CAS number 96610-56-9, is an organic compound that serves as a versatile intermediate in various chemical reactions and processes. It is characterized by its unique structure, which includes a ketone group (-Oxo), a propyl chain, and an ester functional group. This combination of functional groups endows it with a wide range of reactivity and potential applications in different industries.

96610-56-9

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96610-56-9 Usage

Uses

Used in Organic Synthesis:
3-Oxo-2-propylheptanoic Acid Ethyl Ester is used as a synthetic intermediate for the production of various organic compounds. Its presence of a ketone group and ester functionality allows it to participate in a variety of chemical reactions, such as reduction, oxidation, and esterification, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Oxo-2-propylheptanoic Acid Ethyl Ester is used as a key intermediate in the synthesis of drug molecules. Its unique structure can be modified and functionalized to create new compounds with potential therapeutic properties. It may be used in the development of drugs targeting various diseases and conditions, including but not limited to, pain management, inflammation, and infectious diseases.
Used in Agrochemical Industry:
3-Oxo-2-propylheptanoic Acid Ethyl Ester also finds application in the agrochemical industry, where it is used as a precursor in the synthesis of pesticides, herbicides, and other crop protection agents. Its ability to be modified and incorporated into complex molecules makes it a valuable component in the development of new and effective agrochemicals.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, 3-Oxo-2-propylheptanoic Acid Ethyl Ester can be used as a starting material for the synthesis of various aroma chemicals and flavor compounds. Its unique structure can be manipulated to create a wide range of scents and tastes, contributing to the development of new and innovative products in this industry.
Used in Material Science:
3-Oxo-2-propylheptanoic Acid Ethyl Ester can also be utilized in the field of material science, where it may be used as a component in the synthesis of polymers, coatings, and other materials. Its versatility in chemical reactions allows it to be incorporated into the development of new materials with improved properties, such as enhanced durability, stability, or specific functional characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 96610-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,1 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96610-56:
(7*9)+(6*6)+(5*6)+(4*1)+(3*0)+(2*5)+(1*6)=149
149 % 10 = 9
So 96610-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O3/c1-4-7-9-11(13)10(8-5-2)12(14)15-6-3/h10H,4-9H2,1-3H3

96610-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-oxo-2-propylheptanoate

1.2 Other means of identification

Product number -
Other names 2-Valeryl-valeriansaeure-ethylester

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:96610-56-9 SDS

96610-56-9Downstream Products

96610-56-9Relevant academic research and scientific papers

Solvent-free Claisen and Cannizzaro reactions

Yoshizawa, Kazuhiro,Toyota, Shinji,Toda, Fumio

, p. 7983 - 7985 (2007/10/03)

Claisen and Cannizzaro reactions were found to proceed efficiently under solvent-free conditions. The solvent-free Claisen reactions were especially effective for the ester substituted with sterically bulky groups, which does not react in solution.

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