68298-29-3

Usage

Uses

Used in Chemical Synthesis:
(3-methylbutoxy)acetic acid is used as a building block in the synthesis of esters, which are important in the production of fragrances and flavorings. Its reactivity and functional groups make it a versatile component in organic chemistry.
Used in Perfumery:
(3-methylbutoxy)acetic acid is used as a solvent in the perfume industry for blending and stabilizing various aromatic compounds. Its solubility properties and faint fruity odor contribute to the creation of complex and long-lasting fragrances.
Used in Pharmaceutical Production:
(3-methylbutoxy)acetic acid is utilized in the development and manufacturing of pharmaceuticals, where it may serve as an intermediate in the synthesis of active pharmaceutical ingredients or as a component in formulations to improve solubility and bioavailability.
Used in Solvent Applications:
As a solvent, (3-methylbutoxy)acetic acid is employed in various industrial processes, including the cleaning of equipment and the dissolution of other chemicals for further processing or analysis.
It is important to handle (3-methylbutoxy)acetic acid with care and to follow safety regulations when using it due to its potential hazards.

InChI:InChI=1/C7H14O3/c1-6(2)3-4-10-5-7(8)9/h6H,3-5H2,1-2H3,(H,8,9)

Upstream product

• 123-51-3 i-Amyl alcohol 
• 105-36-2 ethyl bromoacetate 
• 623-73-4 diazoacetic acid ethyl ester 
• 79-11-8 chloroacetic acid 
• 19533-24-5 sodium isopentoxide 

Downstream Products

• 67634-00-8 isopentyloxy acetic acid allyl ester 

Relevant academic research and scientific papers

Synthetic method of propylene isopentoxy acetate perfume

The invention discloses a synthetic method of propylene isopentoxy acetate perfume. According to the invention, a Williamson reaction is replaced, and ethyl diazoacetate and isoamyl alcohol are subjected to an O-H insertion reaction under the catalytic action of the catalyst Rh2(OAc)4 to synthesize propylene isopentoxy acetate, so reaction time is greatly shortened; in addition, the prepared solidacid catalyst Yb-MoO3/Al2O3-ZrO2 has the advantages easy separation from a liquid-phase reaction system, no corrosion to equipment and simple aftertreatment, overcomes the problems that conventionalliquid acid corrodes equipment and acid-containing wastewater pollutes environment, and also has high selectivity; the synthetic method can be carried out at low temperature, reduces energy consumption and side reactions, and greatly improves production efficiency; the yield of the prepared propylene isopentoxy acetate perfume is as high as 98.4%; the propylene isopentoxy acetate perfume has goodheat stability, small possibility of loss of active components and good repeated use performance, and is a novel green catalytic material with great application potential.

Pyrimidine derivatives as ghrelin receptor modulators

The present invention is related to compounds of formula (I), or a therapeutically suitable salt or prodrug thereof, the preparation of the compounds, compositions containing the compounds and the use of the compounds in the prevention or treatment of disorders regulated by ghrelin including anorexia, cancer cachexia, eating disorders, age-related decline in body composition, weight gain, obesity, and diabetes mellitus.

Diaminopyrimidine derivatives as growth hormone secrectgogue receptor (GHS-R) antagonists

The present invention is related to compounds of formula (I), or a therapeutically suitable salt or prodrug thereof, the preparation of the compounds, compositions containing the compounds and the use of the compounds in the prevention or treatment of disorders regulated by the action of ghrelin receptor, including Prader-Willi syndrome, eating disorder, weight gain, weight-loss maintainance following diet and exercise, obesity, and disorders associated with obesity such as noninsulin dependent diabetes mellitus.

SULFURIC ACID CATALYZED DECARBONYLATION OF ALKOXYACETYL CHLORIDES

Sulfuric acid catalyzes the decarbonylation of alkoxyacetyl chlorides to produce the corresponding chloromethyl alkyl ethers in fairly good yields.