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2774-84-7,MFCD00041675
Catalog No.:AA002UK6

2774-84-7 | Undec-10-yn-1-ol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$14.00   $10.00
- +
1g
98%
in stock  
$29.00   $21.00
- +
5g
98%
in stock  
$111.00   $78.00
- +
25g
98%
in stock  
$441.00   $309.00
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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:
AA002UK6
Chemical Name:
Undec-10-yn-1-ol
CAS Number:
2774-84-7
Molecular Formula:
C11H20O
Molecular Weight:
168.2759
MDL Number:
MFCD00041675
SMILES:
OCCCCCCCCCC#C
Properties
Properties
 
BP:
243.8°C at 760 mmHg  
Form:
Liquid  
MP:
10.3°C (estimate)  
Refractive Index:
n20/D 1.457  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
120  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
8  
XLogP3:
4.3  

Downstream Synthesis Route

[1]Bedard,Anne-Catherine;Collins,ShawnK.[JournaloftheAmericanChemicalSociety,2011,vol.133,#49,p.19976-19981]

[2]Cheng,Xiamin;Li,Lin;Uttamchandani,Mahesh;Yao,ShaoQ.[OrganicLetters,2014,vol.16,#5,p.1414-1417]

[3]Wapenaar,Hannah;VanDerWouden,PetraE.;Groves,MatthewR.;Rotili,Dante;Mai,Antonello;Dekker,FrankJ.[EuropeanJournalofMedicinalChemistry,2015,vol.105,p.289-296]

[4]Vinczer,Peter;Baan,Gabor;Juvancz,Zoltan;Novak,Lajos;Szantay,Csaba[SyntheticCommunications,1985,vol.15,#14,p.1257-1270]

[5]Ishchenko[ChemistryofNaturalCompounds,1996,vol.32,#1,p.77-79]

[6]Sharma;Chattopadhyay[JournalofOrganicChemistry,1998,vol.63,#18,p.6128-6131]

[7]Knapp,F.F.;Goodman,M.M.;Callahan,A.P.;Ferren,L.A.;Kabalka,G.W.;Sastry,K.A.R.[JournalofMedicinalChemistry,1983,vol.26,#9,p.1293-1300]

[8]Bergel'son,L.D.etal.[JournalofgeneralchemistryoftheUSSR,1962,vol.32,p.57-62][ZhurnalObshcheiKhimii,1962,vol.32,#1,p.58-64]

[9]Ranganathan,S.;Maniktala,Vibha;Kumar,Raaj;Singh,G.P.[IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1984,vol.23,#12,p.1197-1207]

[10]Osskerko[ChemischeBerichte,1937,vol.70,p.56][ZhurnalObshcheiKhimii,vol.7,p.596][ChemischesZentralblatt,1937,vol.108,#II,p.1360]

[11]Han,Bin;Hu,Ping;Wang,Bi-Qin;Redshaw,Carl;Zhao,Ke-Qing[BeilsteinJournalofOrganicChemistry,2013,vol.9,p.2852-2861]

[12]CurrentPatentAssignee:UNIVERSITYOFCOLORADO(SYSTEM);IMMODULONTHERAPEUTICSLTD-US2018/185317,2018,A1

[13]Fang,Ming-Yu;Huang,Kuan-Hsun;Tu,Wei-Ju;Chen,Yi-Ting;Pan,Pei-Yun;Hsiao,Wan-Chi;Ke,Yi-Yu;Tsou,LunK.;Zhang,MingziM.[RedoxBiology,2021,vol.46]

[1]Igner,Eva;Paynter,OliverI.;Simmonds,DerekJ.;Whiting,MarkC.[JournaloftheChemicalSociety.PerkintransactionsI,1987,p.2447-2454]

[1]Neunhoeffer,Hans;Reichel,Diethard;Cullmann,Birgit;Rehn,Ingrid[LiebigsAnnalenderChemie,1990,#7,p.631-640]

[1]Tetrahedron,1997,vol.53,p.1505-1522

[1]Mowery,MarkD.;Evans,ChristineE.[TetrahedronLetters,1997,vol.38,#1,p.11-14]

Literature

Title: Regiospecific identification of 2-(12-ricinoleoylricinoleoyl)-1,3-diricinoleoyl-sn-glycerol in castor (Ricinus communis L.) oil by ESI-MS(4).

Journal: Journal of agricultural and food chemistry 20080528

Title: Improvement of antifungal activity of 10-undecyn-1-ol by inclusion complexation with cyclodextrin derivatives.

Journal: Journal of agricultural and food chemistry 20080528

Title: Synthesis and biological evaluation of new niphathesine analogues.

Journal: Archiv der Pharmazie 20070301

Title: New total synthesis of niphatesine C and norniphatesine C based on a Sonogashira reaction.

Journal: Archiv der Pharmazie 20040701

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SDS
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