2-FURANPROPANOL, alpha-METHYL-

Base Information

• Chemical Name: 2-FURANPROPANOL, alpha-METHYL-
• CAS No.: 6963-39-9
• Molecular Formula: C₈H₁₂O₂
• Molecular Weight: 140.182
• NSC Number: 53774
• DSSTox Substance ID: DTXSID501318847
• Nikkaji Number: J49.600F
• Mol file: 6963-39-9.mol

Synonyms:4-(furan-2-yl)butan-2-ol;6963-39-9;alpha-Methyl-2-furanpropanol;2-FURANPROPANOL, alpha-METHYL-;NSC 53774;BRN 0081113;2-Furanpropanol, .alpha.-methyl-;5-17-03-00403 (Beilstein Handbook Reference);WLN: T5OJ B2YQ1;NSC53774;1-(a-furyl)-3-butanol;SCHEMBL21717728;alpha-Methyl-2-furan-1-propanol;DTXSID501318847;NSC-53774;AKOS009540696;LS-70556;CS-0278606;EN300-1231989

Chemical Property of 2-FURANPROPANOL, alpha-METHYL-

Chemical Property:

• Vapor Pressure: 0.0845mmHg at 25°C
• Boiling Point: 215.9°Cat760mmHg
• Flash Point: 84.4°C
• PSA: 33.37000
• Density: 1.031g/cm³
• LogP: 1.59300
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 140.083729621
• Heavy Atom Count: 10
• Complexity: 93.3

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CCC1=CC=CO1)O

Technology Process of 2-FURANPROPANOL, alpha-METHYL-

There total 35 articles about 2-FURANPROPANOL, alpha-METHYL- 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: 86.0%

4-(furan-2-yl)but-3-en-2-one (623-15-4) → 4-(furan-2-yl)butan-2-ol (6963-39-9,71638-59-0)

Guidance literature:

With hydrogen; In ethanol; at 140 ℃; under 3750.38 Torr; Autoclave;

DOI:10.1002/cssc.201100361

Reference yield: 75.0%

3,4-dibromo-4-furan-2-yl-butan-2-one → 4-(furan-2-yl)butan-2-ol (6963-39-9,71638-59-0)

Guidance literature:

With sodium tetrahydroborate; nickel dichloride; In methanol; at 20 ℃; for 0.75h;

DOI:10.1139/V06-125

Reference yield: 73.0%

4-(furan-2-yl)butan-2-one (699-17-2) → 4-(furan-2-yl)butan-2-ol (6963-39-9,71638-59-0)

Guidance literature:

With sodium tetrahydroborate; In ethanol; for 0.5h;

DOI:10.1039/c2cy20395b

upstream raw materials:

4-(furan-2-yl)butan-2-one

(E)-4-(furan-2-yl)but-3-en-2-one

furan

4-iodo-butan-2-ol

Downstream raw materials:

octane-1,4,7-triol

2-methoxy-7-methyl-1,6-dioxa-spiro[4.4]non-3-ene

4-tetrahydrofuran-2-yl-butan-2-ol

N-(2,2-dichlorovinyl)-N-(3-furan-2-yl-1-methylpropyl)-4-methylbezenesulfonamide

Refernces

• 1、 Chen, Manyu,Xia, Jie,Li, Huan,Zhao, Xiuge,Peng, Qingpo,Wang, Jiajia,Gong, Honghui,Dai, Sheng,An, Pengfei,Wang, Haifeng,Hou, Zhenshan. "A Cationic Ru(II) Complex Intercalated into Zirconium Phosphate Layers Catalyzes Selective Hydrogenation via Heterolytic Hydrogen Activation". . p. 3801 - 3814. Retrieved 2021/08/03.
• 2、 Ramos, Rubén,Ti?ler, Zdeněk,Kikhtyanin, Oleg,Kubi?ka, David. "Solvent effects in hydrodeoxygenation of furfural-acetone aldol condensation products over Pt/TiO2 catalyst". . p. 174 - 183. Retrieved 2016/12/06.