2-(3-Acetylaminophenyl)phenol

Base Information

Chemical Name:2-(3-Acetylaminophenyl)phenol
CAS No.:1261896-19-8
Molecular Formula:C₁₄H₁₃NO₂
Molecular Weight:227.263
Hs Code.:
DSSTox Substance ID:DTXSID40683533
Wikidata:Q82608571

Synonyms:2-(3-ACETYLAMINOPHENYL)PHENOL;1261896-19-8;DTXSID40683533;MFCD18312904;N-(2'-Hydroxy[1,1'-biphenyl]-3-yl)acetamide

Suppliers and Price of 2-(3-Acetylaminophenyl)phenol

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-(3-Acetylaminophenyl)phenol

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:227.094628657
Heavy Atom Count:17
Complexity:267

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=CC=CC(=C1)C2=CC=CC=C2O

Technology Process of 2-(3-Acetylaminophenyl)phenol

There total 1 articles about 2-(3-Acetylaminophenyl)phenol 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: 58.0%

: 533-58-4
2-Iodophenol

: 78887-39-5
3-Acetamidophenylboronic acid

: 1261896-19-8
C₁₄H₁₃NO₂

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; In 1,4-dioxane; water; at 100 ℃; Inert atmosphere;
DOI:10.1055/s-0031-1290966

Reference yield: 69.0%

: 1261896-19-8
C₁₄H₁₃NO₂

: 50548-37-3
N-(4-dibenzofuranyl)acetamide

Guidance literature:: With copper diacetate; caesium carbonate; Trimethylacetic acid; In dimethyl sulfoxide; at 140 ℃; for 24h; regioselective reaction; Inert atmosphere;
DOI:10.1055/s-0031-1290966