11-Aminoundecan-1-ol

Base Information

• Chemical Name: 11-Aminoundecan-1-ol
• CAS No.: 27780-89-8
• Molecular Formula: C11H25NO
• Molecular Weight: 187.326
• European Community (EC) Number: 817-108-6
• Nikkaji Number: J1.175.996C
• Mol file: 27780-89-8.mol

Synonyms:11-aminoundecan-1-ol;11-Amino-1-undecanol;27780-89-8;11-amino-undecanol;SCHEMBL2007847;QCSCNTGILDKNRW-UHFFFAOYSA-N;CBA78089;MFCD09923493;AKOS006311539;AB92460;EN300-219317;F80233;Z1198263294

Chemical Property of 11-Aminoundecan-1-ol

Chemical Property:

• Melting Point: 71-73 °C
• Boiling Point: 286.5±13.0 °C(Predicted)
• PKA: 15.20±0.10(Predicted)
• PSA: 46.25000
• Density: 0.886±0.06 g/cm3(Predicted)
• LogP: 3.14860
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 10
• Exact Mass: 187.193614421
• Heavy Atom Count: 13
• Complexity: 86.2

Purity/Quality:

99% ^*data from raw suppliers

11-aminoundecan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C(CCCCCN)CCCCCO

Technology Process of 11-Aminoundecan-1-ol

There total 10 articles about 11-Aminoundecan-1-ol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

11-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-undecanol (99824-42-7) → 11-aminoundecan-1-ol (27780-89-8)

Guidance literature:

With hydrazine hydrate; In ethanol; at 0 ℃; for 3.25h; Reflux; Inert atmosphere;

DOI:10.1021/ma300090a

Reference yield: 75.0%

11-aminoundecanoic acid (2432-99-7,25587-80-8,84029-94-7) → 11-aminoundecan-1-ol (27780-89-8)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at -20 - 70 ℃; for 48.5h; Inert atmosphere;

DOI:10.1021/jm401586a

Reference yield:

methyl 10-cyano-2-decenoate (1226980-96-6) → 11-aminoundecan-1-ol (27780-89-8)

Guidance literature:

With platinum(IV) oxide; hydrogen; acetyl chloride; In methanol; at 20 ℃; for 24h; under 15001.5 Torr;

upstream raw materials:

tetrachloromethane

ethanol

11-bromoundecan-1-amine

methyl 11-aminoundecanoate

Downstream raw materials:

11-(5,6-Diphenyl-[1,2,4]triazin-3-ylamino)-undecan-1-ol

{2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester

{2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(E)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester

11-aminoundecanoic acid

Refernces

• 1、 Niwa, Masazo,Morikawa, Masa-Aki,Nabeta, Tomohiro,Higashi, Nobuyuki. "Preparation of anthryl group-tagged helical poly(γ-benzyl L-glutamate) self-assembled film on gold surface and its interaction with DNA". . p. 2769 - 2775. Retrieved 2002.
• 2、 Zhao, Jun,Zhang, Zhaoming,Cheng, Lin,Bai, Ruixue,Zhao, Dong,Wang, Yongming,Yu, Wei,Yan, Xuzhou. "Mechanically Interlocked Vitrimers". supporting information. p. 872 - 882. Retrieved 2022/01/03.
• 3、 Jiang, Bing,Zhao, Meng,Li, Shu-Sen,Xu, Yun-He,Loh, Teck-Peng. "Macrolide Synthesis through Intramolecular Oxidative Cross-Coupling of Alkenes". supporting information. p. 555 - 559. Retrieved 2018/02/21.