(2,5-Dimethylfuran-3-yl)methanol

Base Information

• Chemical Name: (2,5-Dimethylfuran-3-yl)methanol
• CAS No.: 1003-96-9
• Molecular Formula: C7H10O2
• Molecular Weight: 126.1531
• Hs Code.: 2932190090
• European Community (EC) Number: 861-594-2
• DSSTox Substance ID: DTXSID00439154
• Wikidata: Q82255047
• ChEMBL ID: CHEMBL4540364
• Mol file: 1003-96-9.mol

Synonyms:(2,5-dimethylfuran-3-yl)methanol;1003-96-9;(2,5-dimethyl-3-furyl)methanol;2,5-dimethyl-3-furanmethanol;SCHEMBL3100001;CHEMBL4540364;DTXSID00439154;YZKVNZQOYBRCPL-UHFFFAOYSA-N;2,5-dimethyl-3- hydroxymethylfuran;MFCD11646256;STL388007;AKOS009358521;AS-49349;CS-0280239;EN300-108594;H10999

Chemical Property of (2,5-Dimethylfuran-3-yl)methanol

Chemical Property:

• PSA: 33.37000
• LogP: 1.38870
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 126.068079557
• Heavy Atom Count: 9
• Complexity: 92.9

Purity/Quality:

97% ^*data from raw suppliers

(2,5-Dimethylfuran-3-yl)methanol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=C(O1)C)CO

Technology Process of (2,5-Dimethylfuran-3-yl)methanol

There total 4 articles about (2,5-Dimethylfuran-3-yl)methanol 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%

2,5-dimethyl-furan-3-carbonyl chloride (50990-93-7) → 2,5-dimethyl-3-(hydroxymethyl)furan (1003-96-9)

Guidance literature:

2,5-dimethyl-furan-3-carbonyl chloride; With sodium tetrahydroborate; In tetrahydrofuran; at 0 ℃;

With hydrogenchloride; water; In tetrahydrofuran;

Reference yield: 95.0%

ethyl 2,5-dimethyl-3-furoate (29113-63-1) → 2,5-dimethyl-3-(hydroxymethyl)furan (1003-96-9)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; for 10h; Ambient temperature;

DOI:10.1021/jo00088a054

Reference yield:

methyl 2,5-dimethylfuran-3-carboxylate (6148-34-1) → 2,5-dimethyl-3-(hydroxymethyl)furan (1003-96-9)

Guidance literature:

With hydrogenchloride; diisobutylaluminium hydride; In dichloromethane;

upstream raw materials:

ethyl 2,5-dimethyl-3-furoate

methyl 2,5-dimethylfuran-3-carboxylate

2,5-dimethyl-furan-3-carbonyl chloride

Downstream raw materials:

(2,5-Dimethyl-3-furyl)methyl benzoate

dimethyl-2,5 formyl-3 furanne