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623-93-8,MFCD00021944
Catalog No.:AA003MUT

623-93-8 | 5-Nonanol

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Purity
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Price(USD)
Quantity
  
1g
98%
in stock  
$36.00   $25.00
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5g
98%
in stock  
$58.00   $40.00
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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:
AA003MUT
Chemical Name:
5-Nonanol
CAS Number:
623-93-8
Molecular Formula:
C9H20O
Molecular Weight:
144.2545
MDL Number:
MFCD00021944
SMILES:
CCCCC(CCCC)O
NSC Number:
4552
Properties
Properties
 
BP:
193.0°C  
Form:
Liquid  
MP:
5℃  

Computed Properties
 
Complexity:
53.7  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
6  
XLogP3:
3.2  

Downstream Synthesis Route

[1]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn11;14

[2]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn10;14

[3]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn11;14

[4]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn11;14

[5]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn10;14

[6]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn13-14

[7]JournaloftheAmericanChemicalSociety,2009,vol.131,p.251-262

[8]JournalofOrganicChemistry,2014,vol.79,p.6094-6104

[9]JournalofOrganicChemistry,1986,vol.51,p.5482-5484

[10]Organometallics,2013,vol.32,p.660-664

[11]JournalofChemicalResearch-PartS,2002,p.508-510

[12]OrganicLetters,2015,vol.17,p.3326-3329

[13]GreenChemistry,2019,vol.21,p.5896-5903

[14]ChemicalCommunications,2011,vol.47,p.1875-1877

[15]ChemSusChem,2013,vol.6,p.1774-1778

[16]OrganicPreparationsandProceduresInternational,1992,vol.24,p.363-365

[17]ACSCatalysis,2018,vol.8,p.5425-5430

[18]DaltonTransactions,2018,vol.47,p.16534-16542

[19]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn13-14

[20]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn13-14

[21]JournaloftheAmericanChemicalSociety,1946,vol.68,p.1372

[22]JournalofOrganicChemistry,1980,vol.45,p.5269-5273

[23]TetrahedronLetters,1999,vol.40,p.3723-3726

[24]JournaloftheIndianChemicalSociety,2002,vol.79,p.815-818

[25]PolishJournalofChemistry,2005,vol.79,p.1963-1965

[26]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,2006,vol.45,p.2441-2445

[27]RussianChemicalBulletin,2010,vol.59,p.391-395

[28]RussianChemicalBulletin,2010,vol.59,p.1284-1288

[29]JournalofCatalysis,2013,vol.300,p.242-250

[30]AdvancedSynthesisandCatalysis,2013,vol.355,p.2591-2603

[31]CatalysisCommunications,2014,vol.47,p.58-62

[32]AsianJournalofChemistry,2014,vol.26,p.2702-2706

[33]ChemicalCommunications,2019,vol.55,p.13610-13613

[1]TetrahedronLetters,1989,vol.30,p.4275-4278

[2]TetrahedronLetters,1989,vol.30,p.4275-4278

[1]Kossanyi;Sabbah;Chaquin;Ronfart-Haret[Tetrahedron,1981,vol.37,#19,p.3307-3315]

[1]JournalofChemicalResearch,Miniprint,2000,p.701-715

[1]Patent:JP2005/524706,2005,A.Locationinpatent:Page/Pagecolumn26-27

Literature

Title: Effect of the addition of alkanols of different topology to dipalmitoyl-phosphatidylcholine vesicles in the presence of gramicidin.

Journal: Journal of colloid and interface science 20121101

Title: Sampling and characterisation of volatile organic compound profiles in human saliva using a polydimethylsiloxane coupon placed within the oral cavity.

Journal: The Analyst 20120821

Title: Creating space for large secondary alcohols by rational redesign of Candida antarctica lipase B.

Journal: Chembiochem : a European journal of chemical biology 20050601

Title: Solvent effect on ion-pair extraction of 2-(2-pyridylazo)-1-naphthol-4-sulfonate anion with solvated hydroxonium ion using alcohols and 1-octanol/octane mixed solvents.

Journal: Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20010201

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