10-Undecen-1-ol - ≥98% , CAS No.112-43-6

CAS: 112-43-6 Cat. No.: U106482 Peso molecular: 170.29 Beilstein Registry Number: 1753225 Número EC: 203-971-0 PubChem CID: 8185

GRADE & PURITY ≥98%

Synonyms

omega-Undecylenyl alcohol | 10-Undecylen-1-ol | undec-10-en-1-ol | WLN: Q10U1 | 1-Undecen-11-ol | Q18611668 | omega-undecylenyl alcoho | SY011350 | Undec-10-enol | omega-Undecenyl alcohol | AI3-06259 | AKOS015903579 | DTXSID4059419 | .OMEGA.-UNDECENOL | 1

Storage

Room temperature

Shipped In

Normal

Application

228,229

Descripción general

application：

10-Undecen-1-ol is used as a flavoring agent. It reacts with tosylated beta-cyclodextrin to prepare beta-cyclodextrin undecenylether. It is used in the synthesis of 10-Undecenylacrylat by reacting with acryloyl and triethylamine. It reacts with carbon monoxide in the presence of dicobalt octacarbonyl and pyridine as a base at pressures greater than 150 bar and temperatures in the range of 100 to 2000C to linear and branched polyesters having relatively high molecular weights (Mn> 10,000 g / mol) in good yields.

Specifications

Sinónimos

omega-Undecylenyl alcohol | 10-Undecylen-1-ol | undec-10-en-1-ol | WLN: Q10U1 | 1-Undecen-11-ol | Q18611668 | omega-undecylenyl alcoho | SY011350 | Undec-10-enol | omega-Undecenyl alcohol | AI3-06259 | AKOS015903579 | DTXSID4059419 | .OMEGA.-UNDECENOL | 1

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488180722
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180722
• Sonrisas canónicas: C=CCCCCCCCCCO
• IUPAC Name: undec-10-en-1-ol
• InChIKey: GIEMHYCMBGELGY-UHFFFAOYSA-N
• INCHI: 1S/C11H22O/c1-2-3-4-5-6-7-8-9-10-11-12/h2,12H,1,3-11H2
• Isómeros SMILES: C=CCCCCCCCCCO
• WGK Alemania: 2
• RTECS: YQ2985000
• PubChem CID: 8185
• Peso molecular: 170.29
• Beilstein: 1753225
• Reaxy-Rn: 1753225

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty alcohols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty alcohols
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty alcohols
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: Miscible with alcohol and ether. Immiscible with water
• Índice de refracción: 1.446-1.453
• Punto de inflamación (°F): 257 °F
• Punto de inflamación (°C): 93℃
• Punto de ebullición (°C): 245-248°C
• Punto de fusión (°C): -3°C
• Peso molecular: 170.290 g/mol
• XLogP3: 4.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• Exact Mass: 170.167 Da
• Monoisotopic Mass: 170.167 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 89.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Xuan Xin, Mengmeng Zhang, Xiao-Feng Li, Guanglei Zhao.  (2019)  Biocatalytic Synthesis of Lipophilic Baicalin Derivatives as Antimicrobial Agents.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:31564105] [10.1021/acs.jafc.9b04667]

2. Changchang Zhang, Yong Kuai, Heming Cheng, Xiang Liu, Liang Ma.  (2017)  Covalent bonding of grafted polymer brushes of poly(poly(ethylene glycol) monomethacrylate) on surface of silicon quantum dots and the activation of the end hydroxyls.  Arabian Journal of Chemistry,      [PMID:] [10.1016/j.arabjc.2016.12.022]

3. Chenyang Xia, Bowen Lu, Qi Xu, Nanxin Shen, Qiancheng Liao, Jiyun Cui, Baiyang Wang, Yueyang Sun, Changjiang Dong, Fei Gan.  (2025)  Structural and Mechanistic Insights into Dual Deprotonation by an Engineered GPP Methyltransferase: Discovery of Methyltransferases Generating Noncanonical Prenyl Diphosphates.  ACS Catalysis,      [PMID:] [10.1021/acscatal.5c03939]