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2-Ethylbenzenecarboximidamide

Base Information
  • Chemical Name:2-Ethylbenzenecarboximidamide
  • CAS No.:184778-41-4
  • Molecular Formula:C9H12N2
  • Molecular Weight:148.208
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30399050
  • Wikidata:Q82201373
  • Mol file:184778-41-4.mol
2-Ethylbenzenecarboximidamide

Synonyms:2-ethylbenzenecarboximidamide;184778-41-4;2-ethylbenzamidine;2-ethylbenzene-1-carboximidamide;2-Ethylbenzimidamide;SCHEMBL10805483;DTXSID30399050;AKOS011677822;CS-0306049;FT-0765129;EN300-1829103

Suppliers and Price of 2-Ethylbenzenecarboximidamide
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
  • Labseeker
  • 2-Ethyl-Benzamidine0 95
  • 10g
  • $ 2163.00
  • American Custom Chemicals Corporation
  • 2-ETHYL-BENZAMIDINE 95.00%
  • 5MG
  • $ 502.11
  • AHH
  • 2-ethylbenzamidine 97%
  • 5g
  • $ 1100.00
Total 7 raw suppliers
Chemical Property of 2-Ethylbenzenecarboximidamide
Chemical Property:
  • Boiling Point:252.5±33.0 °C(Predicted) 
  • PKA:12.02±0.40(Predicted) 
  • PSA:49.87000 
  • Density:1.04±0.1 g/cm3(Predicted) 
  • LogP:2.33310 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:148.100048391
  • Heavy Atom Count:11
  • Complexity:143
Purity/Quality:

98%Min *data from raw suppliers

2-Ethyl-Benzamidine0 95 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=CC=CC=C1C(=N)N
Technology Process of 2-Ethylbenzenecarboximidamide

There total 2 articles about 2-Ethylbenzenecarboximidamide 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:
Multi-step reaction with 2 steps
1: 40 percent / NH2OH*HCl, K2CO3 / aq. ethanol / 41 h / Heating
2: 1.) Ac2O, 2.) H2 / 1.) Pd-C / 1.) glac. AcOH, 5 min, 2.) 4 h
With hydroxylamine hydrochloride; hydrogen; acetic anhydride; potassium carbonate; palladium on activated charcoal; In ethanol;
DOI:10.1080/00397919608003838
Guidance literature:
With hydrogen; acetic anhydride; palladium on activated charcoal; Yield given. Multistep reaction; 1.) glac. AcOH, 5 min, 2.) 4 h;
DOI:10.1080/00397919608003838
upstream raw materials:

o-ethylbenzonitrile

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