1191-16-8 | Prenyl acetate

Packsize	Purity	Availability	Price	Discounted Price
25g	97%	in stock	$19.00	$14.00
100g	97%	in stock	$27.00	$19.00

Description

• Catalog Number: AA23373
• Chemical Name: Prenyl acetate
• CAS Number: 1191-16-8
• Molecular Formula: C7H12O2
• Molecular Weight: 128.169
• MDL Number: MFCD00036569
• SMILES: CC(=O)OCC=C(C)C

Computed Properties

• Complexity: 121
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 1.8

Upstream Synthesis Route

3-Methylbut-2-en-1-yl acetate, also known as isopentenyl acetate, is a versatile compound commonly used in chemical synthesis. This compound is valued for its applications in organic chemistry, particularly in the synthesis of various pharmaceuticals, fragrances, and flavoring agents. In chemical reactions, 3-Methylbut-2-en-1-yl acetate can serve as a precursor for the preparation of other important compounds. Its unique structure and reactivity make it a valuable building block for creating complex molecules with specific properties and functionalities. Additionally, its pleasant fruity odor makes it a preferred choice for incorporation into perfumes and other scented products. In summary, 3-Methylbut-2-en-1-yl acetate plays a crucial role in the synthesis of a wide range of compounds, contributing to advancements in various industries.

Literature

• Defensive compounds and male-produced sex pheromone of the stink bug, Agroecus griseus.

  Journal of chemical ecology 20120901

• An alarm pheromone modulates appetitive olfactory learning in the honeybee (apis mellifera).

  Frontiers in behavioral neuroscience 20100101

• Behavioral genomics of honeybee foraging and nest defense.

  Die Naturwissenschaften 20070401

• Discovery of 3-methyl-2-buten-1-yl acetate, a new alarm component in the sting apparatus of Africanized honeybees.

  Journal of chemical ecology 20030201

• An X-ray study of the effect of the bite angle of chelating ligands on the geometry of palladium(allyl) complexes: implications for the regioselectivity in the allylic alkylation.

  Inorganic chemistry 20010702