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Encyclopedia

Benzadox

Base Information Edit
  • Chemical Name:Benzadox
  • CAS No.:5251-93-4
  • Molecular Formula:C9H9 N O4
  • Molecular Weight:195.175
  • Hs Code.:2924299090
  • European Community (EC) Number:226-053-1
  • NSC Number:75601
  • UNII:KSR5R1E31I
  • DSSTox Substance ID:DTXSID7041625
  • Nikkaji Number:J8.827G
  • Wikidata:Q27282415
  • Metabolomics Workbench ID:143694
  • ChEMBL ID:CHEMBL449455
  • Mol file:5251-93-4.mol
Benzadox

Synonyms:Benzadox;5251-93-4;2-benzamidooxyacetic acid;Topicide;Topcide;(Benzamidooxy)acetic acid;Benzamidoxyacetic acid;Acetic acid, (benzamidooxy)-;(Benzamido)oxy Acetic Acid;Benzamidooxyacetic acid;o-Benzamidoglycolic acid;Acetic acid, [(benzoylamino)oxy]-;NSC 75601;Benzadox [ANSI];S 6173;((Benzoylamino)oxy)acetic acid;[(Benzoylamino)oxy]acetic acid;Caswell No. 075C;Hydroxylamine, N-benzoyl-O-(carboxymethyl)-;Benzadox [ANSI:BSI];S-7173;S-7,173;UNII-KSR5R1E31I;(Benzamido)oxyAceticAcid-d2;KSR5R1E31I;DTXSID7041625;EINECS 226-053-1;NSC-75601;EPA Pesticide Chemical Code 275400;S 7173;Acetic acid, ((benzoylamino)oxy)-;2-(Benzamidooxy)aceticacid;(Benzoylaminooxy)acetic acid;NCIOpen2_000731;SCHEMBL132682;CHEMBL449455;DTXCID5021625;NSC75601;2-[(phenylformamido)oxy]acetic acid;Tox21_301883;AKOS009021683;NCGC00160576-01;NCGC00255650-01;2-((BENZOYLAMINO)OXY)ACETIC ACID;CAS-5251-93-4;Acetic acid, ((benzoylamino)oxy)- (9CI);Acetic acid, (benzamidooxy)- (7CI)(8CI);FT-0662533;ACETIC ACID, 2-((BENZOYLAMINO)OXY)-;S-6173;Q27282415

Suppliers and Price of Benzadox
Supply Marketing:Edit
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
  • TRC
  • (Benzamido)oxyAceticAcid
  • 250 mg
  • $ 1320.00
  • Medical Isotopes, Inc.
  • (Benzamido)oxyAceticAcid
  • 250 mg
  • $ 2200.00
  • Biosynth Carbosynth
  • (Benzamido)oxy acetic acid
  • 50 mg
  • $ 496.00
  • Biosynth Carbosynth
  • (Benzamido)oxy acetic acid
  • 25 mg
  • $ 272.50
  • Biosynth Carbosynth
  • (Benzamido)oxy acetic acid
  • 10 mg
  • $ 149.90
  • Biosynth Carbosynth
  • (Benzamido)oxy acetic acid
  • 100 mg
  • $ 901.00
  • Biosynth Carbosynth
  • (Benzamido)oxy acetic acid
  • 250 mg
  • $ 1640.00
  • American Custom Chemicals Corporation
  • BENZADOX 98.00%
  • 1G
  • $ 958.65
  • American Custom Chemicals Corporation
  • (BENZAMIDO)OXY ACETIC ACID 95.00%
  • 5MG
  • $ 497.95
Total 8 raw suppliers
Chemical Property of Benzadox Edit
Chemical Property:
  • Melting Point:140°C 
  • Refractive Index:1.5700 (estimate) 
  • Boiling Point:°Cat760mmHg 
  • PKA:2.75±0.10(Predicted) 
  • Flash Point:°C 
  • PSA:75.63000 
  • Density:1.325g/cm3 
  • LogP:0.82350 
  • Solubility.:Methanol 
  • Water Solubility.:15.75g/L(temperature not stated) 
  • XLogP3:-0.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:195.05315777
  • Heavy Atom Count:14
  • Complexity:211
Purity/Quality:

99% *data from raw suppliers

(Benzamido)oxyAceticAcid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=O)NOCC(=O)O
  • Uses Hippurate analog. Inhibitor of peptidylglycine α-hydroxylating monooxygenase (PHM). Pesticide.
Technology Process of Benzadox

There total 11 articles about Benzadox 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 hydrogenchloride; sodium hydroxide; chloroacetic acid; In methanol; ethyl acetate;
Guidance literature:
With sodium hydroxide; In water; at 20 ℃;
DOI:10.1016/j.bmcl.2009.11.056
Refernces Edit
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