2-[N-(o-Methylphenyl)carbamoyl]-3-naphthyl acetate

Base Information

• Chemical Name: 2-[N-(o-Methylphenyl)carbamoyl]-3-naphthyl acetate
• CAS No.: 528-66-5
• Molecular Formula: C20H17 N O3
• Molecular Weight: 319.36
• European Community (EC) Number: 208-439-1
• DSSTox Substance ID: DTXSID70200777
• Nikkaji Number: J182.292F
• Wikidata: Q83073944
• Mol file: 528-66-5.mol

Synonyms:528-66-5;Naphthol AS-D acetate;2-[N-(o-Methylphenyl)carbamoyl]-3-naphthyl acetate;3-(o-tolylcarbamoyl)naphthalen-2-yl acetate;[3-[(2-methylphenyl)carbamoyl]naphthalen-2-yl] acetate;EINECS 208-439-1;2-(N-(o-Methylphenyl)carbamoyl)-3-naphthyl acetate;Naphthol-AS-D-acetat;C20H17NO3;3-(Acetyloxy)-N-(2-methylphenyl)-2-naphthalenecarboxamide;DTXSID70200777;MFCD00042713;AKOS015903058;AS-82854;[3-(o-tolylcarbamoyl)-2-naphthyl] acetate;3-(o-tolylcarbamoyl)naphthalen-2-ylacetate;CS-0453357;FT-0632306;E79420;A829287;3-Acetoxy-N-(2-methylphenyl)-2-naphthalenecarboxamide

Chemical Property of 2-[N-(o-Methylphenyl)carbamoyl]-3-naphthyl acetate

Chemical Property:

• Vapor Pressure: 4.07E-12mmHg at 25°C
• Melting Point: 167-169 °C
• Boiling Point: 549.3 °C at 760 mmHg
• PKA: 12.67±0.70(Predicted)
• Flash Point: 286 °C
• Density: 1.252 g/cm³
• Storage Temp.: 2-8°C
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 319.12084340
• Heavy Atom Count: 24
• Complexity: 464

Purity/Quality:

98%min ^*data from raw suppliers

NAPHTHOL AS-D ACETATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=CC=CC=C1NC(=O)C2=CC3=CC=CC=C3C=C2OC(=O)C

Technology Process of 2-[N-(o-Methylphenyl)carbamoyl]-3-naphthyl acetate

There total 1 articles about 2-[N-(o-Methylphenyl)carbamoyl]-3-naphthyl acetate 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:

→ 2-[N-(o-methylphenyl)carbamoyl]-3-naphthyl acetate (528-66-5)

Guidance literature:

2-Hydroxy-naphthalin-3-carbonsaeure-o-toluidid in sd. Py. u. Acetanhydrid;