2-chloro-N-(4-phenoxyphenyl)acetamide

Base Information

• Chemical Name: 2-chloro-N-(4-phenoxyphenyl)acetamide
• CAS No.: 36160-84-6
• Molecular Formula: C14H12ClNO2
• Molecular Weight: 261.708
• Hs Code.: 2924299090
• European Community (EC) Number: 635-712-6
• DSSTox Substance ID: DTXSID40353148
• Nikkaji Number: J1.124.516A
• Wikidata: Q82130604
• ChEMBL ID: CHEMBL2164311
• Mol file: 36160-84-6.mol

Synonyms:2-chloro-N-(4-phenoxyphenyl)acetamide;36160-84-6;MFCD00028181;SCHEMBL3382618;CHEMBL2164311;DTXSID40353148;PHUZNDQAFGNCRQ-UHFFFAOYSA-N;STK395083;AKOS000268699;N-(4-phenoxyphenyl)-2-chloro-acetamide;2-Chloro-N-4-(4-phenoxyphenyl)acetamide;BS-11082;CS-0307510;FT-0639304;EN300-01555;Z56813578

Chemical Property of 2-chloro-N-(4-phenoxyphenyl)acetamide

Chemical Property:

• Vapor Pressure: 6.14E-08mmHg at 25°C
• Refractive Index: 1.619
• Boiling Point: 439.9 °C at 760 mmHg
• Flash Point: 219.8 °C
• PSA: 38.33000
• Density: 1.279 g/cm³
• LogP: 3.72920
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 261.0556563
• Heavy Atom Count: 18
• Complexity: 259

Purity/Quality:

98%min ^*data from raw suppliers

2-CHLORO-N-(4-PHENOXYPHENYL)ACETAMIDE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)OC2=CC=C(C=C2)NC(=O)CCl

Technology Process of 2-chloro-N-(4-phenoxyphenyl)acetamide

There total 2 articles about 2-chloro-N-(4-phenoxyphenyl)acetamide 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: 95.0%

chloroacetyl chloride (79-04-9) + 4-phenoxyanilin (139-59-3) → 2-chloro-N-(4-phenoxyphenyl)acetamide (36160-84-6)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 1h;

Reference yield: 46.0%

→ 2-chloro-N-(4-phenoxyphenyl)acetamide (36160-84-6)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;

Reference yield: 92.0%

2-chloro-N-(4-phenoxyphenyl)acetamide (36160-84-6) + 1-[5-(phenoxy)pentyl]uracil (28484-92-6) → 2-[2,6-dioxo-3-(5-phenoxypentyl)-3,6-dihydropyrimidin-1(2H)-yl]-N-(4-phenoxyphenyl)acetamide

Guidance literature:

1-[5-(phenoxy)pentyl]uracil; With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 0.666667h;

2-chloro-N-(4-phenoxyphenyl)acetamide; In N,N-dimethyl-formamide; at 20 ℃; for 24h;

DOI:10.1016/j.bmc.2015.09.033

upstream raw materials:

chloroacetyl chloride

4-phenoxyanilin

Downstream raw materials:

thiocyanato-acetic acid-(4-phenoxy-anilide)

2-(2-hydroxyethylamino)-N-(4-phenoxyphenyl)acetamide

2--N-(4-phenoxyphenyl)acetamide

N-(4-Phenoxy-phenyl)-2-piperidin-1-yl-acetamide; compound with oxalic acid

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