1,3-Benzenediol, 5-(2-propenyloxy)-

Base Information

• Chemical Name: 1,3-Benzenediol, 5-(2-propenyloxy)-
• CAS No.: 813414-06-1
• Molecular Formula: C9H10O3
• Molecular Weight: 166.177
• DSSTox Substance ID: DTXSID60461870
• Nikkaji Number: J2.108.375E
• Wikidata: Q82286315

Synonyms:1,3-Benzenediol, 5-(2-propenyloxy)-;813414-06-1;SCHEMBL16015475;DTXSID60461870

Chemical Property of 1,3-Benzenediol, 5-(2-propenyloxy)-

Chemical Property:

• XLogP3: 1.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 166.062994177
• Heavy Atom Count: 12
• Complexity: 137

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 1,3-Benzenediol, 5-(2-propenyloxy)-

There total 2 articles about 1,3-Benzenediol, 5-(2-propenyloxy)- 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: 85.0%

3,5-dihydroxyphenol (108-73-6) + 3-chloroprop-1-ene (107-05-1) → 1-(2-propenyloxy)-3,5-dihydroxybenzene (813414-06-1)

Guidance literature:

With zinc; In N,N-dimethyl-formamide; for 0.0833333h; microwave irradiation;

DOI:10.1016/j.tetlet.2004.10.009

Reference yield: 60.0%

3,5-dihydroxyphenol (108-73-6) → 1-(2-propenyloxy)-3,5-dihydroxybenzene (813414-06-1)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1016/j.bmc.2006.10.006

Reference yield: 95.0%

1-(2-propenyloxy)-3,5-dihydroxybenzene (813414-06-1) → 5-propoxybenzene-1,3-diol (77173-35-4)

Guidance literature:

With 5%-palladium/activated carbon; hydrogen; In ethanol; at 20 ℃; for 12h;

DOI:10.1021/ol303019q

upstream raw materials:

3,5-dihydroxyphenol

3-chloroprop-1-ene

Downstream raw materials:

2,4-Diacetyl-5-allyl-resorcinol

1-(2-propenyloxy)-4-acetyl-3,5-dihydroxybenzene

5-propoxybenzene-1,3-diol

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