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29548-30-9,MFCD00036516
Catalog No.:AA002YMZ

29548-30-9 | Farnesyl acetate

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1g
95%
in stock  
$37.00   $26.00
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5g
95%
in stock  
$79.00   $55.00
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25g
95%
in stock  
$195.00   $137.00
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100g
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$643.00   $450.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002YMZ
Chemical Name:
Farnesyl acetate
CAS Number:
29548-30-9
Molecular Formula:
C17H28O2
Molecular Weight:
264.4030
MDL Number:
MFCD00036516
SMILES:
CC(=CCCC(=CCOC(=O)C)C)CCC=C(C)C
NSC Number:
132958
FEMA Number:
4213
Properties
Properties
 
BP:
115-125 °C0.3 mm Hg(lit.)  
Refractive Index:
n20/D 1.477  
Storage:
-20 ℃;  

Computed Properties
 
Complexity:
356  
Covalently-Bonded Unit Count:
1  
Defined Bond Stereocenter Count:
2  
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
9  
XLogP3:
5.3  

Downstream Synthesis Route

[1]Fischer,F.G.[JustusLiebigsAnnalenderChemie,1928,vol.464,p.82,86]

[1]Tetrahedron,2014,vol.70,p.9718-9725

105-83-9    29548-30-9   
{3-(3-aminopropyl)methylaminopropyl}(3,7,11-trimethyldodeca-2,6,10-trienyl)amine 

[1]Tetrahedron,2014,vol.70,p.9718-9725

[1]Synlett,2017,vol.28,p.2665-2669

Literature

Title: The geranyl-modified tryptophan residue is crucial for ComXRO-E-2 pheromone biological activity.

Journal: Bioorganic & medicinal chemistry letters 20110701

Title: 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.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20091109

Title: A two-component female-produced pheromone of the spider Pholcus beijingensis.

Journal: Journal of chemical ecology 20090701

Title: Screening of terpenes and derivatives for antimycobacterial activity; identification of geranylgeraniol and geranylgeranyl acetate as potent inhibitors of Mycobacterium tuberculosis in vitro.

Journal: Planta medica 20071001

Title: Identification of pheromones and optimization of bait composition for click beetle pests (Coleoptera: Elateridae) in Central and Western Europe.

Journal: Pest management science 20030401

Title: Guo D, et al. Biosynthesis of advanced biofuel farnesyl acetate using engineered Escherichia coli. Bioresour Technol. 2018 Dec;269:577-580.

Title: Hussain A, et al. Lethality of Sesquiterpenes Reprogramming Red Palm Weevil Detoxification Mechanism for Natural Novel Biopesticide Development. Molecules. 2019 Apr 26;24(9).

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SDS
Tags:29548-30-9 Molecular Formula|29548-30-9 MDL|29548-30-9 SMILES|29548-30-9 Farnesyl acetate