trans,trans-Farnesyl acetate - CAS 4128-17-0

Catalog:	BB024846
Product Name:	trans,trans-Farnesyl acetate
CAS:	4128-17-0
Synonyms:	0

Technical Data

Patents

Literatures

Computed Properties

IUPAC Name:	[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate
Description:	trans,trans-Farnesyl acetate (CAS# 4128-17-0) is an intermediate in the synthesis of JHSB3 (J211030). JHSB3 is an acyclic sesquiterpenoid that regulates many aspects of insect physiology. Juvenile Hormone regulate development, reproduction, diapause, and polyphenisms.
Molecular Weight:	264.40
Molecular Formula:	0
Canonical SMILES:	0
InChI:	0
InChI Key:	0
Boiling Point:	145 ℃ (4 mmHg)
Density:	0.908-0.914
Solubility:	Practically insoluble to insoluble in water
Appearance:	Colorless liquid
LogP:	4.96870

Publication Number	Title	Priority Date
DE-102020204506-A1	Fabric softener with pheromones	20200407
CN-111272906-A	Method for determining flower fragrance components in main stream smoke of cigarette	20200331
CN-110604133-A	Gathering pheromone and lure of common thrips and application thereof	20190822
WO-2020249707-A1	Granular detergent-, cleaning agent- or treatment agent additive	20190613
CN-112585117-A	Method for synthesizing vitamin A	20180820

PMID	Publication Date	Title	Journal
21636272	20110701	The geranyl-modified tryptophan residue is crucial for ComXRO-E-2 pheromone biological activity	Bioorganic & medicinal chemistry letters
21480512	20110401	Chemical constituents and antimicrobial activity of the leaf and rhizome oils of Alpinia pahangensis Ridl., an endemic wild ginger from peninsular Malaysia	Chemistry & biodiversity
19780112	20091109	Acid-catalyzed cyclization of terpenes under homogeneous and heterogeneous conditions as probed through stereoisotopic studies: a concerted process with competing preorganized chair and boat transition states	Chemistry (Weinheim an der Bergstrasse, Germany)
19579045	20090701	A two-component female-produced pheromone of the spider Pholcus beijingensis	Journal of chemical ecology
17482441	20080101	Chemical composition and antimicrobial activity of volatile components from capitula and aerial parts of Rhaponticum acaule DC growing wild in Tunisia	Microbiological research

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Related Functional Groups

Carbonyl Compounds

[87-88-7]
Chloranilic acid
[1427004-19-0]
DBCO-PEG4-NHS ester
[70199-62-1]
(4-Pyridyl)acetone Hydrochloride
[1018141-88-2]
1-(2-Cyanoethyl)-3-methyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid
[55441-25-3]
1-(2-Cyanophenyl)urea
[1035840-45-9]
1-(5-Methoxy-1,3-benzoxazol-2-yl)piperidine-3-carboxylic acid

Complexity:	356
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	2
Exact Mass:	264.208930132
Formal Charge:	0
Heavy Atom Count:	19
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	264.208930132
Rotatable Bond Count:	9
Topological Polar Surface Area:	26.3
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	5.3