7785-66-2

Usage

Uses

Used in Fragrance and Flavor Industry:
Butyl tiglate is used as a key ingredient in the formulation of fragrances and flavors due to its appealing scent, enhancing the sensory experience of various products.
Used in Chemical Processes:
In the chemical industry, butyl tiglate serves as a solvent, facilitating various chemical reactions and processes, thereby contributing to the efficiency and effectiveness of these operations.
Used in Food Industry:
As a flavoring agent, butyl tiglate is incorporated into the food industry to impart a pleasant taste to different food products, enhancing their overall flavor profile.
Safety Note:
It is crucial to handle butyl tiglate with caution due to its potential to cause irritation to the skin, eyes, and respiratory system upon exposure, emphasizing the need for proper safety measures during its use.

InChI:InChI=1S/C9H16O2/c1-4-6-7-11-9(10)8(3)5-2/h5H,4,6-7H2,1-3H3/b8-5+

Upstream product

• 590-19-2 2,3-dimethylbutene 
• 201230-82-2 carbon monoxide 
• 71-36-3 butan-1-ol 
• 80-59-1 Tiglic acid 

Downstream Products

• 1380708-61-1 (Z)-butyl 3-(3-bromo-5-(trifluoromethyl)phenyl)-2-methylbut-2-enoate 
• 1380708-62-2 (Z)-butyl 3-(3-bromo-5-chlorophenyl)-2-methylbut-2-enoate 
• 1380708-60-0 (Z)-butyl 3-(3-bromophenyl)-2-methylbut-2-enoate 
• 1380708-77-9 (Z)-butyl 3-(4-bromophenyl)-2-methylbut-2-enoate 

Relevant academic research and scientific papers

Ligand-Controlled Palladium-Catalyzed Alkoxycarbonylation of Allenes: Regioselective Synthesis of α,β- and β,γ-Unsaturated Esters

The palladium-catalyzed regioselective alkoxycarbonylation of allenes with aliphatic alcohols allows to produce synthetically useful α,β- and β,γ-unsaturated esters in good yields. Efficient selectivity control is achieved in the presence of appropriate ligands. Using Xantphos as the ligand, β,γ-unsaturated esters are produced selectively in good yields. In contrast, the corresponding α,β-unsaturated esters are obtained with high regioselectivity in the presence of PPh2Py as the ligand. Preliminary mechanistic studies revealed that these two catalytic processes proceed by different reaction pathways. In addition, this novel protocol was successfully applied to convert an industrially available bulk chemical, 1,2-butadiene, into dimethyl adipate, which is a valuable feedstock for polymer and plasticizer syntheses, with high yield and TON (turnover number).

Undirected arene and chelate-assisted olefin C-H bond activation: [Rh IIICp*]-catalyzed dehydrogenative alkene-arene coupling as a new pathway for the selective synthesis of highly substituted Z olefins

Undirected/Directed Cross-Coupling: A new dehydrogenative Rh III-catalyzed cross-coupling reaction between bromoarenes bearing no directing group and vinylic substrates substituted by a chelating group is reported. An original reaction mechanism enables the use of internal alkenes in a Z-selective coupling. The application of 1,3-disubstituted or 1,2-homodisubstituted arenes leads to the formation of highly functionalized, complex, and valuable olefins as one single isomer. Copyright

ENZYMATIC ENANTIOSELECTIVE HYDROLYSIS OF 2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLIC ESTERS

2,2-dimethyl-1,3-dioxolane-4-carboxylic acid derived chiral building blocks were prepared from substituted α,β-unsaturated acids with high enantiomeric purities by enzymatic hydrolysis of their n.butyl esters.