30414-54-1    
 
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CAS 30414-54-1 Methyl 3-oxohexanoate | Products & Prices & Suppliersts

Methyl 3-oxohexanoate, with the chemical formula C7H12O3, has the CAS number 30414-54-1. It is a chemical compound that appears as a colorless liquid with a fruity odor. The basic structure of Methyl 3-oxohexanoate consists of a methyl group attached to a carbon chain with a carbonyl group at the third position. This compound is soluble in organic solvents but sparingly soluble in water. Safety information regarding Methyl 3-oxohexanoate is not available.

Applicable Fields

Fragrance: Methyl 3-oxohexanoate is commonly used in the fragrance industry. Its purpose in this field is to provide a fruity scent to various products. The mechanism of action in fragrance involves the release of volatile compounds that contribute to the desired aroma.

Flavoring: This chemical compound is also utilized as a flavoring agent. Its purpose in the food industry is to enhance the taste of certain products. The mechanism of action in flavoring involves the interaction of Methyl 3-oxohexanoate with taste receptors, resulting in a specific flavor perception.

Storage

Conditions: Store in a cool and dry place.

ldentification

Cas NO.: 30414-54-1
CID: 121700
Mw: 144.17
MF: C7H12O3
Name:Methyl 3-oxohexanoate (Related Reference)
Synonyms: 3-KETOHEXANOIC ACID METHYL ESTER; 3-KETO-N-HEXANOIC ACID METHYL ESTER; 3-OXOHEXANOIC ACID METHYL ESTER; 3-Oxo-hexanoic acid methyl ester; 3V1VO1; BEM; BUTYRYLACETIC ACID METHYL ESTER;
EINECS: 250-185-9

Safety Data

[Safety Statements] S24/25:Avoid contact with skin and eyes
Hazard Symbols:

Properties

Appearance:Colorless transparent liquid
Molecular Weight:144.17
Density:1.017
Boiling Point:85-88℃
Melting Point:-43°C
Flash Point:73.2 °C
Refractive index:1.4260
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Methyl butyrylacetate
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Butyrylacetic acid methyl ester
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Question & Answer
What is the synthesis method of Methyl 3-oxohexanoate and its applications? Background and Overview[1] Methyl 3-oxohexanoate is an organic intermediate that has been reported in the literature to be used for the preparation of 4(3H)-quinazolinone derivatives. 4(3H)-quinazolin.. Feb 27 2021
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