(4-Hydroxy-3,5-dimethoxyphenyl)(3-hydroxy-4-morpholinyl)methanone

Base Information

Chemical Name:(4-Hydroxy-3,5-dimethoxyphenyl)(3-hydroxy-4-morpholinyl)methanone
CAS No.:76534-75-3
Molecular Formula:C₁₃H₁₇NO₆
Molecular Weight:283.281
Hs Code.:
DSSTox Substance ID:DTXSID901167779

Synonyms:DTXSID901167779;(4-Hydroxy-3,5-dimethoxyphenyl)(3-hydroxy-4-morpholinyl)methanone;76534-75-3

Suppliers and Price of (4-Hydroxy-3,5-dimethoxyphenyl)(3-hydroxy-4-morpholinyl)methanone

Supply Marketing:

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

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Chemical Property of (4-Hydroxy-3,5-dimethoxyphenyl)(3-hydroxy-4-morpholinyl)methanone

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:283.10558726
Heavy Atom Count:20
Complexity:325

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC(=CC(=C1O)OC)C(=O)N2CCOCC2O

Technology Process of (4-Hydroxy-3,5-dimethoxyphenyl)(3-hydroxy-4-morpholinyl)methanone

There total 3 articles about (4-Hydroxy-3,5-dimethoxyphenyl)(3-hydroxy-4-morpholinyl)methanone 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: 41.0%

: 76534-74-2
2-<2-(3,5-dimethoxy-4-hydroxybenzamido)ethoxy>-1,1-diethoxyethane

: 76534-75-3
4-(3,5-dimethoxy-4-hydroxybenzoyl)-3-morpholinol

Guidance literature:: With oxalic acid; In water; acetone; at 60 ℃; for 120h;

Reference yield:

: 39657-47-1
O-acetylsyringic acid chloride

: 76534-75-3
4-(3,5-dimethoxy-4-hydroxybenzoyl)-3-morpholinol

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / triethylamine / CH₂Cl₂

2: 96 percent / 7percent sodium carbonate / H₂O / 1 h / 50 °C

3: 41 percent / oxalic acid / H₂O; acetone / 120 h / 60 °C

With oxalic acid; sodium carbonate; triethylamine; In dichloromethane; water; acetone;

Reference yield:

: 76534-73-1
2-<2-(4-acetoxy-3,5-dimethoxybenzamido)ethoxy>-1,1-diethoxyethane

: 76534-75-3
4-(3,5-dimethoxy-4-hydroxybenzoyl)-3-morpholinol

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / 7percent sodium carbonate / H₂O / 1 h / 50 °C

2: 41 percent / oxalic acid / H₂O; acetone / 120 h / 60 °C

With oxalic acid; sodium carbonate; In water; acetone;