ETHYL 2-METHYL-3-PENTENOATE

  • Name: ETHYL 2-METHYL-3-PENTENOATE
  • CAS: 1617-23-8
  • Purity: 99%
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What is the ETHYL 2-METHYL-3-PENTENOATE ?

ETHYL 2-METHYL-3-PENTENOATE is Colorless liquid, while it's Molecular Formula is C8H14O2. Used in Flavor and Fragrance Industry:
ETHYL 2-METHYL-3-PENTENOATE is used as a flavoring agent for its sweet, ripe fruity taste, resembling apple, pineapple, and strawberry with hints of melon. It is particularly useful in the creation of flavors for the food and beverage industry.
ETHYL 2-METHYL-3-PENTENOATE is also used as a fragrance ingredient for its sweet estry, fresh, and juicy fruity aroma with green and slightly pungent notes of apple, pear, banana, pineapple, and tutti-frutti. It is commonly utilized in the perfumery and cosmetics industry to create captivating and long-lasting scents.
Used in the Chemical Industry:
In the chemical industry, ETHYL 2-METHYL-3-PENTENOATE can be used as an intermediate in the synthesis of various chemicals and materials, taking advantage of its unique chemical structure and properties.

What is the CAS number for ETHYL 2-METHYL-3-PENTENOATE ?

The CAS number of ETHYL 2-METHYL-3-PENTENOATE is 1617-23-8.

More information of ETHYL 2-METHYL-3-PENTENOATE 1617-23-8 are:

Synonyms

Ethyl2-methyl-3-pentenoate;Ethyl oxanoate 369;

CAS?Number

1617-23-8

Molecular Formula

C8H14O2

Molecular Weight

142.198

Density

0.899 g/cm3

Boiling Point

163.2 °C at 760 mmHg

Flash Point

59.1 °C

HS CODE

2916190090

PSA

26.30000

LogP

1.76170

What is ETHYL 2-METHYL-3-PENTENOATE (1617-23-8) used for?

ETHYL 2-METHYL-3-PENTENOATE is an organic compound with a distinctive sweet, ripe fruity aroma and taste. It is characterized by its apple, pineapple, and strawberry-like flavor with hints of melon, and a sweet estry, fresh, and juicy fruity aroma with green and slightly pungent notes of apple, pear, banana, pineapple, and tutti-frutti.

InChI:InChI=1/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h4,6-7H,5H2,1-3H3/b6-4+

Articles related to ETHYL 2-METHYL-3-PENTENOATE:

Article

Source

Selective Isomerization of Terminal Alkenes to (Z)-2-Alkenes Catalyzed by an Air-Stable Molybdenum(0) Complex

Becica, Joseph,Glaze, Owen D.,Wozniak, Derek I.,Dobereiner, Graham E.

, p. 482 - 490 (2018/02/17)

Ether carbinols and process for preparing same

-

, (2008/06/13)

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