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N-(2-bromoethyl)benzamide

Base Information
  • Chemical Name:N-(2-bromoethyl)benzamide
  • CAS No.:27110-61-8
  • Molecular Formula:C9H10 Br N O
  • Molecular Weight:228.088
  • Hs Code.:2924299090
  • European Community (EC) Number:808-812-4
  • NSC Number:71031
  • DSSTox Substance ID:DTXSID40290786
  • Nikkaji Number:J3.602.071G
  • Wikidata:Q82028574
  • Mol file:27110-61-8.mol
N-(2-bromoethyl)benzamide

Synonyms:N-(2-bromoethyl)benzamide;27110-61-8;NSC71031;NCIOpen2_003226;N-(2-Bromoethyl)-benzamide;SCHEMBL1337737;DTXSID40290786;WCTQETQDPVEMGT-UHFFFAOYSA-N;NSC-71031;AKOS008998749

Suppliers and Price of N-(2-bromoethyl)benzamide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 6 raw suppliers
Chemical Property of N-(2-bromoethyl)benzamide
Chemical Property:
  • Vapor Pressure:5.34E-06mmHg at 25°C 
  • Melting Point:104-105 °C 
  • Boiling Point:380.7°C at 760 mmHg 
  • PKA:13.72±0.46(Predicted) 
  • Flash Point:184.1°C 
  • PSA:29.10000 
  • Density:1.43g/cm3 
  • LogP:2.20220 
  • XLogP3:1.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:226.99458
  • Heavy Atom Count:12
  • Complexity:144
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=O)NCCBr
Technology Process of N-(2-bromoethyl)benzamide

There total 13 articles about N-(2-bromoethyl)benzamide 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:
Guidance literature:
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 6h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.9b01257
Guidance literature:
benzoic acid; With diatomite earth(at)IL/ZrCl4 (Lewis acidic ionic liquid immobilized on diatomite earth); In toluene; for 0.0833333h; Green chemistry;
2-bromoethylamine; In toluene; at 20 ℃; for 0.416667h; Sonication; Green chemistry;
DOI:10.1007/s11164-018-3592-9
Guidance literature:
With triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/acs.orglett.1c01622
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