66576-71-4

Usage

Uses

Used in Flavor Industry:
FEMA 3699 is used as a flavoring agent for its fruity, sweet, apple, pineapple, green, tutti-frutti, and citrus nuances. It is commonly utilized in the creation of various food and beverage products to enhance their taste and aroma.
Used in Fragrance Industry:
FEMA 3699 is used as a fragrance ingredient for its unique combination of fruity, sweet, green, oily, ethereal, and tropical scents with a pineapple nuance. It is often employed in the formulation of perfumes, colognes, and other personal care products to provide a pleasant and long-lasting scent.
Used in Concord Grape and Strawberry Flavors:
FEMA 3699 is specifically used as a flavoring agent in the production of Concord grape and strawberry fruit-flavored products. Its taste and aroma characteristics closely mimic the natural flavors of these fruits, making it an ideal choice for enhancing the overall flavor profile of these products.

InChI:InChI=1/C8H16O2/c1-5-7(4)8(9)10-6(2)3/h6-7H,5H2,1-4H3

Upstream product

• 1733-25-1 isopropyl tiglate 
• 80-59-1 Tiglic acid 
• 201230-82-2 carbon monoxide 
• 67-63-0 isopropyl alcohol 
• 106-97-8 n-butane 

Downstream Products

• 137-32-6 (+/-)-2-methyl-1-butanol 

Relevant academic research and scientific papers

Highly enantioselective iridium-catalyzed hydrogenation of α,β-unsaturated esters

α,β-Unsaturated esters have been employed as substrates in iridium-catalyzed asymmetric hydrogenation. Full conversions and good to excellent enantioselectivities (up to 99 % ee) were obtained for a broad range of substrates with both aromatic- and aliphatic substituents on the prochiral carbon. The hydrogenated products are highly useful as building blocks in the synthesis of a variety of natural products and pharmaceuticals. Asymmetric hydrogenation: A variety of α,β-unsaturated esters were hydrogenated with high enantioselectivities (see scheme). The hydrogenated products have been used in synthetic transformations as well as in formal total syntheses. Copyright

The first examples of selective carbonylation of n-butane and n-pentane

The polyhalomethane based superelectrophilic systems allowed us to accomplish the first efficient and selective carbonylation of n-butane and n- pentane with CO. Depending on the nature of the superelectrophilic system, Me3CCOOR or EtCH(Me)COOR (R = H, Alk) can be obtained at -20°C, 1 atm from n-butane and CO after water (α alcohol) treatment in = 90% yield based on the superelectrophilic system. Pentane reacts with CO in the presence d the CBr4 · 2AlBr3 superacid to give a single product, EtC(Me)2COOR, in almost quantitative yield.