Benzeneacetamide, N-cyclooctyl-4-hydroxy-3-methoxy-

Base Information

Chemical Name:Benzeneacetamide, N-cyclooctyl-4-hydroxy-3-methoxy-
CAS No.:107512-66-3
Molecular Formula:C₁₇H₂₅NO₃
Molecular Weight:291.39
Hs Code.:
DSSTox Substance ID:DTXSID20148074
Nikkaji Number:J562.191G
Wikidata:Q83013522
ChEMBL ID:CHEMBL86481
Mol file:107512-66-3.mol

Synonyms:BRN 2987221;Benzeneacetamide, N-cyclooctyl-4-hydroxy-3-methoxy-;N-Cycloctyl-4-hydroxy-3-methoxybenzeneacetamide;107512-66-3;CHEMBL86481;SCHEMBL9808765;DTXSID20148074;LS-28498;N-Cyclooctyl-4-hydroxy-3-methoxybenzeneacetamide

Suppliers and Price of Benzeneacetamide, N-cyclooctyl-4-hydroxy-3-methoxy-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of Benzeneacetamide, N-cyclooctyl-4-hydroxy-3-methoxy-

Chemical Property:

Vapor Pressure:2.53E-11mmHg at 25°C
Boiling Point:517.4°Cat760mmHg
PKA:9.91±0.20(Predicted)
Flash Point:266.7°C
PSA：62.05000
Density:1.12g/cm³
LogP:4.01270
XLogP3:3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:291.18344366
Heavy Atom Count:21
Complexity:313

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=CC(=C1)CC(=O)NC2CCCCCCC2)O

Technology Process of Benzeneacetamide, N-cyclooctyl-4-hydroxy-3-methoxy-

There total 5 articles about Benzeneacetamide, N-cyclooctyl-4-hydroxy-3-methoxy- 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:

: Acetic acid 4-cyclooctylcarbamoylmethyl-2-methoxy-phenyl ester

: 107512-66-3
N-Cyclooctyl-2-(4-hydroxy-3-methoxy-phenyl)-acetamide

Guidance literature:: With sodium hydroxide; In methanol; for 3h; Yield given; Ambient temperature;
DOI:10.1021/jm00070a002

Reference yield:

: 306-08-1
Homovanillic acid

: 107512-66-3
N-Cyclooctyl-2-(4-hydroxy-3-methoxy-phenyl)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 79 percent / H₂SO₄ / Ambient temperature

2: SOCl₂ / Heating

3: benzene; diethyl ether / 3 h / 0 - 20 °C

4: aq. NaOH / methanol / 3 h / Ambient temperature

With sodium hydroxide; thionyl chloride; sulfuric acid; In methanol; diethyl ether; benzene;
DOI:10.1021/jm00070a002

Reference yield:

: 5447-38-1
2-(4-acetoxy-3-methoxyphenyl)acetic acid

: 107512-66-3
N-Cyclooctyl-2-(4-hydroxy-3-methoxy-phenyl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / Heating

2: benzene; diethyl ether / 3 h / 0 - 20 °C

3: aq. NaOH / methanol / 3 h / Ambient temperature

With sodium hydroxide; thionyl chloride; In methanol; diethyl ether; benzene;
DOI:10.1021/jm00070a002