1,3-Benzenediol, 5-ethoxy-

Base Information

• Chemical Name: 1,3-Benzenediol, 5-ethoxy-
• CAS No.: 28334-98-7
• Molecular Formula: C8H10 O3
• Molecular Weight: 154.166
• Hs Code.: 2909499000
• European Community (EC) Number: 248-973-2
• DSSTox Substance ID: DTXSID2067377
• Nikkaji Number: J250.699H
• Wikidata: Q81993959
• Mol file: 28334-98-7.mol

Synonyms:5-Ethoxyresorcinol;1,3-Benzenediol, 5-ethoxy-;28334-98-7;EINECS 248-973-2;5-ethoxybenzene-1,3-diol;Resorcinol, 5-ethoxy-;5-Ethoxy-1,3-benzenediol;SCHEMBL70827;phloroglucinol monoethyl ether;DTXSID2067377

Chemical Property of 1,3-Benzenediol, 5-ethoxy-

Chemical Property:

• Vapor Pressure: 0.00124mmHg at 25°C
• Boiling Point: 289.8°C at 760 mmHg
• Flash Point: 129.1°C
• PSA: 49.69000
• Density: 1.215g/cm³
• LogP: 1.49650
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 154.062994177
• Heavy Atom Count: 11
• Complexity: 106

Purity/Quality:

99% ^*data from raw suppliers

5-ETHOXYRESORCINOL 97.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC1=CC(=CC(=C1)O)O

Technology Process of 1,3-Benzenediol, 5-ethoxy-

There total 10 articles about 1,3-Benzenediol, 5-ethoxy- 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: 79.0%

→ Phloroglucinmonoethylether (28334-98-7)

Guidance literature:

Reference yield: 43.0%

2-ethoxyprop-1-ene (926-66-9) + malonoyl dichloride (1663-67-8) → 4-hydroxy-6-methyl-2-pyron (675-10-5) + Phloroglucinmonoethylether (28334-98-7)

Guidance literature:

In diethyl ether;

Reference yield: 41.0%

3,5-dihydroxyphenol (108-73-6) + ethyl iodide (75-03-6) → Phloroglucinmonoethylether (28334-98-7)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

upstream raw materials:

3,5-dihydroxyphenol

ethanol

2-ethoxyprop-1-ene

malonoyl dichloride

Downstream raw materials:

3,5-diethoxyphenol

2-ethoxy-4,6-dihydroxy-benzaldehyde

2,3',4'-triethoxy-4,6-dihydroxy-deoxybenzoin

2,3',4'-triethoxy-6-hydroxy-4-methoxy-deoxybenzoin