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(2-Amino-5-methylphenyl)phosphonic acid

Base Information
  • Chemical Name:(2-Amino-5-methylphenyl)phosphonic acid
  • CAS No.:69675-98-5
  • Molecular Formula:C7H10NO3P
  • Molecular Weight:187.135
  • Hs Code.:
  • European Community (EC) Number:839-661-2
  • NSC Number:87208
  • DSSTox Substance ID:DTXSID80293099
  • Nikkaji Number:J3.164.186A
  • Wikidata:Q82031698
(2-Amino-5-methylphenyl)phosphonic acid

Synonyms:(2-amino-5-methylphenyl)phosphonic acid;69675-98-5;NSC87208;(2-amino-5-methyl-phenyl)phosphonic acid;C7H10NO3P;SCHEMBL17607326;DTXSID80293099;MFCD20699745;NSC-87208;AKOS028111199;(2-amino-5-methylphenyl)phosphonicacid;CS-0058758;D83786;EN300-252339

Suppliers and Price of (2-Amino-5-methylphenyl)phosphonic acid
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 8 raw suppliers
Chemical Property of (2-Amino-5-methylphenyl)phosphonic acid
Chemical Property:
  • Vapor Pressure:1.62E-08mmHg at 25°C 
  • Boiling Point:440°Cat760mmHg 
  • Flash Point:219.9°C 
  • Density:1.43g/cm3 
  • XLogP3:0.2
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:187.03983018
  • Heavy Atom Count:12
  • Complexity:203
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C=C1)N)P(=O)(O)O
Technology Process of (2-Amino-5-methylphenyl)phosphonic acid

There total 3 articles about (2-Amino-5-methylphenyl)phosphonic acid 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 trimethylsilyl bromide; In acetonitrile; at 25 ℃; for 16h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 3 steps
1: sodium hydrogencarbonate; iodine / water; dichloromethane / 22 h / 0 - 25 °C / Inert atmosphere
2: potassium carbonate; N,N`-dimethylethylenediamine; copper(l) iodide / toluene / 18 h / 110 °C / Inert atmosphere
3: trimethylsilyl bromide / acetonitrile / 16 h / 25 °C / Inert atmosphere
With copper(l) iodide; trimethylsilyl bromide; iodine; sodium hydrogencarbonate; potassium carbonate; N,N`-dimethylethylenediamine; In dichloromethane; water; toluene; acetonitrile;
Guidance literature:
2-Chlor-5-methyl-phenylphosphonsaeure*H2O, 1) konz. wss. NH3, 2) wss. HCl, H2S;
DOI:10.1021/jo01031a509
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