3-(1-Hydroxyethyl)benzophenone

Base Information

• Chemical Name: 3-(1-Hydroxyethyl)benzophenone
• CAS No.: 67173-18-6
• Molecular Formula: C15H14O2
• Molecular Weight: 226.275
• European Community (EC) Number: 641-463-4
• DSSTox Substance ID: DTXSID40518230
• Nikkaji Number: J2.208.153E
• Mol file: 67173-18-6.mol

Synonyms:3-(1-Hydroxyethyl)benzophenone;67173-18-6;Methanone, [3-(1-hydroxyethyl)phenyl]phenyl-;[3-(1-hydroxyethyl)phenyl]-phenylmethanone;[3-(1-Hydroxyethyl)phenyl]phenylmethanone;3-(1-hydroxvethyl)benzophenone;SCHEMBL4669024;1-(3-benzoylphenyl)ethan-1-ol;DTXSID40518230;VIGLCJZNAGRKFZ-UHFFFAOYSA-N;AKOS028113809;[3-(1-Hydroxyethyl)phenyl](phenyl)methanone

Chemical Property of 3-(1-Hydroxyethyl)benzophenone

Chemical Property:

• Boiling Point: 385.7±25.0 °C(Predicted)
• PKA: 14.15±0.20(Predicted)
• PSA: 37.30000
• Density: 1.139±0.06 g/cm3(Predicted)
• LogP: 2.97090
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility.: Chloroform (Slightly), Ethyl Acetate (Slightly)
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 226.099379685
• Heavy Atom Count: 17
• Complexity: 256

Purity/Quality:

98%Min ^*data from raw suppliers

3-(1-Hydroxyethyl)benzophenone ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C1=CC(=CC=C1)C(=O)C2=CC=CC=C2)O
• Uses: 3-(1-Hydroxyethyl)benzophenone is the photodegradation product of Ibuprofen (I40000) and Ketoprofen (K200800) in aqueous solutions. 3-(1-Hydroxyethyl)benzophenone is the photodegradation product of Ibuprofen (I40000) and Ketoprofen (K200800)in aqueous solutions.

Technology Process of 3-(1-Hydroxyethyl)benzophenone

There total 18 articles about 3-(1-Hydroxyethyl)benzophenone 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: 48.2%

ketoprofen (22071-15-4,22161-86-0) → (3-acetylphenyl)(phenyl)methanone (66067-44-5) + 3-(1-hydroxyethyl)benzophenone (67173-18-6) + 1-chloro-1-(3-benzoylphenyl)ethane (126489-64-3)

Guidance literature:

With (5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato)iron(III) chloride; iodosylbenzene; In dichloromethane; for 20h; Product distribution; Mechanism; Ambient temperature; formation of CO₂ confirmed by FT-IR;

DOI:10.1016/S0040-4039(00)61242-X

Reference yield: 46.0%

ketoprofen (22071-15-4,22161-86-0) → 3-ethylbenzophenone (66067-43-4) + (3-acetylphenyl)(phenyl)methanone (66067-44-5) + 3-(1-hydroxyethyl)benzophenone (67173-18-6) + 2,3-bis-(3-benzoylphenyl)butane + 2-(3-benzoylphenyl)-1-(3-ethylphenyl)-1-phenylpropan-1-ol + 2,2′-((1,2-dihydroxy-1,2-diphenylethane-1,2-diyl)bis(3,1-phenylene))dipropanoic acid

Guidance literature:

With phosphate-buffered saline; deuterated methanol; In water; Product distribution; Irradiation; natural sunlight or pyrex-filtered light of a medium-pressure mercury lamp in oxygen or argon atmosphere at different concentrations;

DOI:10.1111/j.1751-1097.1994.tb05073.x

Reference yield: 46.0%

ketoprofen (22071-15-4,22161-86-0) → 3-ethylbenzophenone (66067-43-4) + 3-(1-hydroxyethyl)benzophenone (67173-18-6) + 2-(3-benzoylphenyl)-1-(3-ethylphenyl)-1-phenylpropan-1-ol + 2,2′-((1,2-dihydroxy-1,2-diphenylethane-1,2-diyl)bis(3,1-phenylene))dipropanoic acid

Guidance literature:

With phosphate-buffered saline; for 1h; Further byproducts given; Irradiation; sunlight;

DOI:10.1111/j.1751-1097.1994.tb05073.x

upstream raw materials:

ketoprofen

1-(3-benzoylphenyl)-1-bromoethane

3-ethylbenzophenone

1,3-dioxoisoindolin-2-yl 2-(3-benzoylphenyl)propanoate

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