trans-2-Nonen-1-ol

Base Information

• Chemical Name: trans-2-Nonen-1-ol
• CAS No.: 31502-14-4
• Molecular Formula: C9H18O
• Molecular Weight: 142.241
• Hs Code.: 2905290000
• European Community (EC) Number: 250-662-1
• UNII: 164F9RI0BJ
• DSSTox Substance ID: DTXSID50885501
• Nikkaji Number: J110.601E,J112.171E
• Wikidata: Q27251778
• Metabolomics Workbench ID: 3221
• ChEMBL ID: CHEMBL2228466
• Mol file: 31502-14-4.mol

Synonyms:trans-2-Nonen-1-ol;31502-14-4;(E)-Non-2-en-1-ol;(E)-2-Nonen-1-ol;2-Nonen-1-ol;trans-2-Nonenol;2-Nonen-1-ol, (2E)-;2-Nonen-1-ol, (E)-;2-nonene-1-ol;FEMA No. 3379;2E-Nonen-1-ol;2-Nonen-1-ol-D2;2-Nonen-1-ol, trans-;(2E)-2-Nonen-1-ol;UNII-164F9RI0BJ;(2E)-non-2-en-1-ol;164F9RI0BJ;trans-2-Nonen-1-ol, 97%;EINECS 250-662-1;AI3-36044;820-25-7;(E)-2-nonenol;(E)-non-2-enol;(2E)-nonen-1-ol;starbld0000855;?trans-2-Nonen-1-ol;SCHEMBL184657;SCHEMBL295668;QSPL 148;CHEMBL2228466;FEMA 3379;DTXSID50885501;CHEBI:142604;NSSALFVIQPAIQK-UHFFFAOYSA-N;LMFA05000131;MFCD00014058;TRANS-2-NONEN-1-OL [FHFI];(E)-2-NONEN-1-OL [FCC];AKOS015902315;HY-W127449;CS-0185681;N0587;trans-2-Nonen-1-ol, >=96%, FCC, FG;D91737;Q27251778

Chemical Property of trans-2-Nonen-1-ol

Chemical Property:

• Vapor Pressure: 0.0368mmHg at 25°C
• Refractive Index: n20/D 1.448(lit.)
• Boiling Point: 213.2 °C at 760 mmHg
• PKA: 14.49±0.10(Predicted)
• Flash Point: 87.3 °C
• PSA: 20.23000
• Density: 0.845 g/cm³
• LogP: 2.50530
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 142.135765193
• Heavy Atom Count: 10
• Complexity: 76.8

Purity/Quality:

99% ^*data from raw suppliers

trans-2-Nonen-1-ol >93.0%(GC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCC=CCO
• Isomeric SMILES: CCCCCC/C=C/CO
• Description: May be synthesized by hydrolysis of the corresponding acetate; the acetate is prepared from l-bromo-2-nonene and acetic anhydride in acetic acid solution.
• Uses: Food additive.

Technology Process of trans-2-Nonen-1-ol

There total 32 articles about trans-2-Nonen-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: 99.0%

2-nonyn-1-ol (5921-73-3) → 2-nonenyl alcohol (31502-14-4)

Guidance literature:

With Red-Al; In diethyl ether; toluene; at 0 - 20 ℃; for 5h; Inert atmosphere;

DOI:10.1021/acs.orglett.8b02568

Reference yield: 93.0%

Diisopropoxy-methyl-((E)-non-2-enyl)-silane (85719-61-5) → 2-nonenyl alcohol (31502-14-4)

Guidance literature:

With potassium fluoride; dihydrogen peroxide; In N,N-dimethyl-formamide; for 40h; Ambient temperature;

DOI:10.1021/jo00160a046

Reference yield: 90.0%

ethyl (2E)-non-2-enoate (38112-59-3) → 2-nonenyl alcohol (31502-14-4)

Guidance literature:

With diisobutylaluminium hydride; In toluene; at 0 ℃; for 1h;

DOI:10.1016/j.tet.2003.09.063

upstream raw materials:

(E)-2-Nonenal

2-nonenyl bromide

(E)-2-nonenoic acid

non-1-ene

Downstream raw materials:

non-2-enal

(E)-non-2-enenitrile

1-{5-[3-(4-methoxybenzyloxy)-propyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-5-methoxymethoxy-undec-1-yn-4-ol

tert-butyl-[4-{5-[3-(4-methoxybenzyloxy)-propyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-1-(1-methoxymethoxyheptyl)-but-3-ynyloxy]-dimethylsilane

Refernces

• 1、 Kuciński, Krzysztof,Hreczycho, Grzegorz. "Lithium triethylborohydride as catalyst for solvent-free hydroboration of aldehydes and ketones". . p. 1912 - 1915. Retrieved 2019/04/27.
• 2、 Li, Hong-Shuang,Guo, Guili,Zhang, Rui-Ze,Li, Fei. "Rhodium-Catalyzed Synthesis of α,β-Unsaturated Ketones through Sequential C-C Coupling and Redox Isomerization". supporting information. p. 5040 - 5043. Retrieved 2018/08/24.