Carbarsone

Base Information

• Chemical Name: Carbarsone
• CAS No.: 121-59-5
• Molecular Formula: C7H9 As N2 O4
• Molecular Weight: 260.081
• Hs Code.: 2931900090
• European Community (EC) Number: 204-484-6
• NSC Number: 759884,32868
• UN Number: 3280
• UNII: 8PK70TXE1T
• DSSTox Substance ID: DTXSID4020246
• Nikkaji Number: J5.340F
• Wikipedia: Carbarsone
• Wikidata: Q5037838
• NCI Thesaurus Code: C76414
• Metabolomics Workbench ID: 152590
• ChEMBL ID: CHEMBL1331366
• Mol file: 121-59-5.mol

Synonyms:4-ureidobenzenearsonic acid;Carbarson;carbarsone;Carbason

Chemical Property of Carbarsone

Chemical Property:

• Melting Point: 174°
• Boiling Point: °Cat760mmHg
• PKA: 3.78±0.10(Predicted)
• Flash Point: °C
• PSA: 112.65000
• Density: g/cm³
• LogP: -0.48850
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 259.977826
• Heavy Atom Count: 14
• Complexity: 256
• Transport DOT Label: Poison

Purity/Quality:

98%min ^*data from raw suppliers

Carbarsone ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC(=CC=C1NC(=O)N)[As](=O)(O)O
• Uses: insecticide, cholinesterase inhibitor

Technology Process of Carbarsone

There total 4 articles about Carbarsone 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:

potassium cyanate (590-28-3) → carbarsone (121-59-5)

Guidance literature:

With acetic acid;

Reference yield:

p-aminophenylarsonic acid (98-50-0) + bromocyane (506-68-3) → carbarsone (121-59-5)

Guidance literature:

With sodium hydroxide;

Reference yield:

p-aminophenylarsonic acid (98-50-0) + bromocyane (506-68-3) → carbarsone (121-59-5)

Guidance literature:

upstream raw materials:

p-aminophenylarsonic acid

bromocyane

potassium cyanate

Downstream raw materials:

p-aminophenylarsonic acid

ammonia

methylammonium carbonate

Refernces