1117-52-8 | Farnesylacetone

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$15.00	$10.00
1g	95%	in stock	$18.00	$12.00
5g	95%	in stock	$25.00	$17.00
10g	95%	in stock	$40.00	$28.00
25g	95%	in stock	$49.00	$34.00
100g	95%	in stock	$175.00	$122.00

Description

• Catalog Number: AI08742
• Chemical Name: Farnesylacetone
• CAS Number: 1117-52-8
• Molecular Formula: C18H30O
• Molecular Weight: 262.4302
• MDL Number: MFCD00036517
• SMILES: CC(=CCC/C(=C/CCC(=O)C)/C)CCC=C(C)C

Computed Properties

• Complexity: 352
• Covalently-Bonded Unit Count: 1
• Defined Bond Stereocenter Count: 2
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• XLogP3: 5.6

Upstream Synthesis Route

The (5E,9E)-6,10,14-Trimethylpentadeca-5,9,13-trien-2-one is a versatile compound commonly used in chemical synthesis as a key building block for creating various organic molecules. Its unique structure and reactivity make it a valuable tool for the synthesis of complex organic compounds such as pharmaceuticals, agrochemicals, and fragrances. The presence of multiple double bonds in the molecule allows for the introduction of various functional groups through chemical reactions, making it an essential component in the creation of structurally diverse compounds. Its role in chemical synthesis extends to the production of natural products, flavors, and fragrance ingredients, showcasing its importance in the field of organic chemistry.

Literature

• Essential oils from stem and leaves of Angelica urumiensis (Mozaffarian) from Iran.

  Natural product research 20100901

• Chemical analysis and biological activity of the essential oils of two endemic Soqotri Commiphora species.

  Molecules (Basel, Switzerland) 20100201

• Chemical composition and phytotoxic effects of essential oils of Salvia hierosolymitana Boiss. and Salvia multicaulis Vahl. var. simplicifolia Boiss. growing wild in Lebanon.

  Molecules (Basel, Switzerland) 20091119

• Vasodilatation effect of farnesylacetones, active constituents of Sargassum siliquastrum, on the basilar and carotid arteries of rabbits.

  Bioorganic & medicinal chemistry letters 20081215

• Cholinesterase inhibitory activity of two farnesylacetone derivatives from the brown alga Sargassum sagamianum.

  Archives of pharmacal research 20031001