Methyl 4-(benzyloxy)-2-hydroxy-6-pentylbenzoate

Base Information

Chemical Name:Methyl 4-(benzyloxy)-2-hydroxy-6-pentylbenzoate
CAS No.:94103-01-2
Molecular Formula:C20H24O4
Molecular Weight:328.408
Hs Code.:
DSSTox Substance ID:DTXSID60552919
Nikkaji Number:J3.400.249E
Wikidata:Q82433332

Synonyms:94103-01-2;Methyl 4-(benzyloxy)-2-hydroxy-6-pentylbenzoate;DTXSID60552919

Suppliers and Price of Methyl 4-(benzyloxy)-2-hydroxy-6-pentylbenzoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Methyl 4-(benzyloxy)-2-hydroxy-6-pentylbenzoate

Chemical Property:

XLogP3:5.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:9
Exact Mass:328.16745924
Heavy Atom Count:24
Complexity:365

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC1=C(C(=CC(=C1)OCC2=CC=CC=C2)O)C(=O)OC

Technology Process of Methyl 4-(benzyloxy)-2-hydroxy-6-pentylbenzoate

There total 2 articles about Methyl 4-(benzyloxy)-2-hydroxy-6-pentylbenzoate 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: 77.0%

: 58016-28-7
methyl 2,6-dihydroxy-6-pentylbenzoate

: 100-39-0
benzyl bromide

: 94103-01-2
methyl 4-benzyloxy-6-hydroxy-2-pentylbenzoate

Guidance literature:: With potassium carbonate; In acetone; for 24h; Heating;

Reference yield:

: 94102-99-5
methyl 4-benzyloxy-2-oxo-6-pentylcyclohex-3-enecarboxylate

: 94103-01-2
methyl 4-benzyloxy-6-hydroxy-2-pentylbenzoate

Guidance literature:: With DBN; bromine; sodium acetate; Yield given. Multistep reaction; 1.) acetic acid, 2.) dichloromethane, room temperature, 24 h;