Arsacetin

Base Information

• Chemical Name: Arsacetin
• CAS No.: 618-22-4
• Molecular Formula: C8H10 As N O4
• Molecular Weight: 259.093
• European Community (EC) Number: 210-541-6
• NSC Number: 62901,13773
• UNII: JS109AD2Z9
• DSSTox Substance ID: DTXSID10210794
• Nikkaji Number: J95.724K
• Wikidata: Q27281659
• ChEMBL ID: CHEMBL1605998
• Mol file: 618-22-4.mol

Synonyms:Arsacetin;N-Acetylarsanilic acid;618-22-4;Arsanilic acid, N-acetyl-;4-Acetamidophenylarsonic acid;(4-(Acetylamino)phenyl)arsonic acid;EINECS 210-541-6;C8H10AsNO4;BRN 3032470;UNII-JS109AD2Z9;MLS000736701;JS109AD2Z9;Acide acetamido-4 benzene arsonique [French];Acide acetamido-4 benzene arsonique;NSC-13773;NSC-62901;Arsonic acid, (4-(acetylamino)phenyl)-;Arsonic acid, [4-(acetylamino)phenyl]-;p-acetamidobenzenearsonic acid;[4-(ACETYLAMINO)PHENYL]ARSONIC ACID;Arsacetin (6CI);ARSACETIN [MI];4-Acetamidobenzolarsonsaure;NCIOpen2_003283;SCHEMBL525047;C8-H10-As-N-O4;CHEMBL1605998;DTXSID10210794;HMS2885B04;NSC13773;NSC62901;NSC 13773;NSC 62901;Arsanilic acid, N-acetyl- (7CI,8CI);NCGC00246853-01;LS-21905;NCI60_000855;SMR000528295;Q27281659

Chemical Property of Arsacetin

Chemical Property:

• PSA: 86.63000
• LogP: -0.72100
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 258.982577
• Heavy Atom Count: 14
• Complexity: 254

Purity/Quality:

98%min ^*data from raw suppliers

ARSACETIN 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1=CC=C(C=C1)[As](=O)(O)O

Technology Process of Arsacetin

There total 7 articles about Arsacetin 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:

→ arsacetin (618-22-4)

Guidance literature:

With sodium hydroxide; trisodium arsenite;

Reference yield:

p-aminophenylarsonic acid (98-50-0) + acetic anhydride (108-24-7) → arsacetin (618-22-4)

Guidance literature:

With sulfuric acid;

Reference yield:

p-aminophenylarsonic acid (98-50-0) + acetyl chloride (75-36-5) → arsacetin (618-22-4)

Guidance literature:

With pyridine;

upstream raw materials:

p-aminophenylarsonic acid

acetic anhydride

acetyl chloride

N-(4-arsorylphenyl)acetamide

Downstream raw materials:

roxarsone