2-Furanmethanol, tetrahydro-alpha-pentyl-

Base Information

• Chemical Name: 2-Furanmethanol, tetrahydro-alpha-pentyl-
• CAS No.: 68480-13-7
• Molecular Formula: C10H20O2
• Molecular Weight: 172.268
• European Community (EC) Number: 270-890-5
• UNII: GNU53V3LL9
• DSSTox Substance ID: DTXSID00887414
• Nikkaji Number: J326.638I
• Mol file: 68480-13-7.mol

Synonyms:68480-13-7;2-Furanmethanol, tetrahydro-alpha-pentyl-;EINECS 270-890-5;2-Furanmethanol, tetrahydro-.alpha.-pentyl-;Tetrahydro-alpha-pentyl-i-furanmethanol;Tetrahydro-alpha-pentyl-2-furanmethanol;Tetrahydro-alpha-pentylfuran-2-methanol;GNU53V3LL9;SCHEMBL4396424;DTXSID00887414;1-(tetrahydrofuran-2-yl)-hexan-1-ol;AKOS014665881;Tetrahydro- alpha-pentylfuran-2-methanol

Chemical Property of 2-Furanmethanol, tetrahydro-alpha-pentyl-

Chemical Property:

• Vapor Pressure: 0.00482mmHg at 25°C
• Boiling Point: 245.3°Cat760mmHg
• Flash Point: 89.5°C
• Density: 0.962g/cm³
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 172.146329876
• Heavy Atom Count: 12
• Complexity: 114

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCC(C1CCCO1)O

Technology Process of 2-Furanmethanol, tetrahydro-alpha-pentyl-

There total 8 articles about 2-Furanmethanol, tetrahydro-alpha-pentyl- 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%

(Z)-4-decen-1-ol (57074-37-0) → threo-1-(2-tetrahydrofuranyl)hexan-1-ol (68480-13-7,143264-37-3,143493-19-0)

Guidance literature:

With Oxone; In water; isopropyl alcohol; at 80 ℃; for 0.0833333h; stereospecific reaction;

DOI:10.3762/bjoc.5.18

Reference yield: 82.0%

(E)-4-decen-1-ol (10339-62-5) → (R)-(S)-1-(Tetrahydro-furan-2-yl)-hexan-1-ol (68480-13-7,143493-19-0,143264-37-3)

Guidance literature:

With dihydrogen peroxide; poly(alkylpyridinium) phosphotungstate; at 50 ℃; for 35h;

DOI:10.1021/ol070258v

Reference yield:

(Z)-4-decen-1-ol (57074-37-0) → (R)-(S)-1-(Tetrahydro-furan-2-yl)-hexan-1-ol (68480-13-7,143493-19-0,143264-37-3)

Guidance literature:

With sodium hydrogensulfite; rhenium(VII) oxide; periodic acid; multistep reaction: oxidative cyclization of 5-hydroxyalkenes with Re₂O₇ utilizing a co-oxidant (H₅IO₆);

DOI:10.1016/S0040-4039(00)79078-2

upstream raw materials:

(Z)-4-decen-1-ol

(E)-4-decen-1-ol

(Z)-4-decenal

Downstream raw materials:

1-acetoxy-1-(2'-tetrahydrofuryl)hexane