2-Decen-1-ol

Base Information

• Chemical Name: 2-Decen-1-ol
• CAS No.: 18409-18-2
• Molecular Formula: C10H20 O
• Molecular Weight: 156.268
• European Community (EC) Number: 242-289-8,244-784-4
• UNII: T46421D2F4
• DSSTox Substance ID: DTXSID701016140
• Nikkaji Number: J285.438D,J82.747I
• Wikidata: Q27289647
• Metabolomics Workbench ID: 3232
• ChEMBL ID: CHEMBL2228372
• Mol file: 18409-18-2.mol

Synonyms:trans-2-Decen-1-ol;2-Decen-1-ol;18409-18-2;(E)-dec-2-en-1-ol;(E)-2-Decenol;trans-2-Decenol;2-Decen-1-ol, (E)-;(E)-2-decen-1-ol;2-Decenol;2-Decenol, (2E)-;Dec-2-enol;22104-80-9;UNII-T46421D2F4;EINECS 242-289-8;T46421D2F4;AI3-36045;Dec-2-en-1-ol;(2E)-2-decenol;E-2-decen-1-ol;Dec-2-en-1-al;2-DECENOL, (E)-;SCHEMBL295757;?TRANS-2-DECEN-1-OL;CHEMBL2228372;FEMA NO. 4304;TRANS-2-DECENOL [FHFI];2-DECEN-1-OL, TRANS-;DTXSID701016140;LMFA05000142;AKOS024387376;J-011793;Q27289647

Chemical Property of 2-Decen-1-ol

Chemical Property:

• Vapor Pressure: 0.000516mmHg at 25°C
• Refractive Index: n20/D 1.451(lit.)
• Boiling Point: 230.3°Cat760mmHg
• PKA: 14.46±0.10(Predicted)
• Flash Point: 96.1°C
• PSA: 20.23000
• Density: 0.845g/cm³
• LogP: 2.89540
• XLogP3: 3.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 156.151415257
• Heavy Atom Count: 11
• Complexity: 86.9

Purity/Quality:

99% ^*data from raw suppliers

trans-2-Decen-1-ol ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCC=CCO
• Isomeric SMILES: CCCCCCC/C=C/CO
• Uses: trans-2-Decen-1-ol is an antibiotic essential oil with nematicidal properties.

Technology Process of 2-Decen-1-ol

There total 26 articles about 2-Decen-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: 100.0%

(E)-2-decenal (3913-81-3) → (E)-2-decenol (18409-18-2)

Guidance literature:

With diisobutylaluminium hydride; In n-heptane; toluene; at -78 ℃; for 2.5h;

DOI:10.3987/com-03-s(p)68

Reference yield: 98.0%

2-decyn-1-ol (4117-14-0) → (E)-2-decenol (18409-18-2)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; for 2h; Heating;

Reference yield: 91.0%

ethyl (E)-2-decenate (7367-88-6) → (E)-2-decenol (18409-18-2)

Guidance literature:

With diisobutylaluminium hydride; In diethyl ether; at 0 ℃;

DOI:10.1021/jo200289f

upstream raw materials:

(2E,7Z)-deca-2,7-dien-1-ol

trans-1-bromo-2-decene

2-decyn-1-ol

2-benzenesulfinyl-decan-1-ol

Downstream raw materials:

2-decenal

3,5-dinitro-benzoic acid dec-2-enyl ester

1-Decanol

(E)-1-benzyloxydec-2-ene

Refernces

• 1、 Mayer, Sandra F.,Steinreiber, Andreas,Orru, Romano V. A.,Faber, Kurt. "Chemoenzymatic asymmetric total syntheses of antitumor agents (3R,9R,10R)- and (3S,9R,10R)-panaxytriol and (R)- and (S)-falcarinol from Panax ginseng using an enantioconvergent enzyme-triggered cascade reaction". . p. 9115 - 9121. Retrieved 2002.
• 2、 Huang, Jiaxin,Li, Jie,Yang, Wen,Zhang, Kezhuo,Zhao, Pei,Zhao, Wanxiang. "Ligand-controlled cobalt-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes". supporting information. p. 302 - 305. Retrieved 2022/01/03.
• 3、 -. "ANTI-BACTERIAL CALCIUM-DEPENDENT ANTIBIOTIC (CDA) ANALOGS AND METHODS OF TREATING BACTERIAL INFECTIONS". Paragraph 0128; 0130. . Retrieved 2021/10/22.