structure of 24323-38-4

Ethyl 2-Hydroxy-3-Methylpentanoate(CAS 24323-38-4)

CAS No.: 24323-38-4 Brand: MolBest
M. Ft.: C8H16O3 Cat. No: G2284391
M. Wt.: 160.21 MDL: No record
Storage: Store in a cool,dry area. Use: For laboratory research use only
Purity Grade Package Stock Price Quantity
97%
Documents:COASDS
RG 100MG In Stock 280 USD
97%
Documents:COASDS
RG 250MG In Stock 504 USD
97%
Documents:COASDS
RG 1G In Stock 1311 USD
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Physical and chemical properties of 24323-38-4

Boiling Point

197.4ºC at 760 mmHg

Density

0.922-0.930

Exact Mass

160.11000

Flash Point

74ºC

Index of Refraction

1.422-1.429

LogP

0.95650

Molecular Formula

C8H16O3

Molecular Weight

160.21100

PSA

46.53000

Solubility

Sparingly soluble (in ethanol)

Vapour Pressure

0.0967mmHg at 25°C

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Q&A for CAS 24323-38-4

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Applications of 24323-38-4

Ethyl 2-hydroxy-3-methylpentanoate has several applications:

  • Fragrance industry: It is used as a perfuming ingredient, imparting a fresh, fruity, walnut-type fragrance with walnut shell notes.
  • Flavor industry: The compound contributes to the aroma profile of various fruits and beverages.
  • Precursor in organic synthesis: It can serve as a starting material for the synthesis of more complex organic compounds.
Similar Compounds

Several compounds share structural similarities with ethyl 2-hydroxy-3-methylpentanoate:

  • Ethyl 2-hydroxy-3-methylbutanoate: This compound differs by one methylene group and is also found in the aroma volatiles of fruits and beverages.
  • 2-Hydroxy-3-methylpentanoic acid: The parent acid of ethyl 2-hydroxy-3-methylpentanoate, involved in isoleucine metabolism.
  • Ethyl 3-methyl-2-oxopentanoate: The oxidized form of ethyl 2-hydroxy-3-methylpentanoate, used as a perfuming ingredient.
  • Ethyl 2-benzyl-3-hydroxy-2-methylpentanoate: A more complex analog with an additional benzyl group.

Ethyl 2-hydroxy-3-methylpentanoate is unique due to its specific fragrance profile and its potential as a versatile synthetic intermediate. Its chirality and the presence of both hydroxyl and ester functional groups contribute to its diverse reactivity and applications in various fields.

Retrosynthesis analysis of 24323-38-4

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