Sulfachrysoidine

Base Information

• Chemical Name: Sulfachrysoidine
• CAS No.: 485-41-6
• Molecular Formula: C13H13 N5 O4 S
• Molecular Weight: 335.343
• European Community (EC) Number: 207-617-6
• UNII: 39O1389K38
• DSSTox Substance ID: DTXSID00871676
• Nikkaji Number: J5.999D
• NCI Thesaurus Code: C72646
• ChEMBL ID: CHEMBL2107474
• Mol file: 485-41-6.mol

Synonyms:Sulfachrysoidine;485-41-6;Rubiazol losung;sulfachrysoidin;Sulfacrisoidina;Sulfachrysoidinum;carboxysulfamidochrysoidine;Collubiazol losung;Azo compd no. 4;3,5-diamino-2-[(4-sulfamoylphenyl)diazenyl]benzoic acid;collubiazol;rubiazole;Sulfachrysoidine [INN:DCF];Sulfachrysoidinum [INN-Latin];Sulfacrisoidina [INN-Spanish];UNII-39O1389K38;EINECS 207-617-6;39O1389K38;2-Carboxy-4,6-diamino-4'-sulfamoylazobenzol;3,5-Diamino-2-(p-sulfamoylphenylazo)benzoic acid;4,6-Diamino-4'-sulfamoylazobenzol-2-carbonsaeure;C13H13N5O4S;3,5-Diamino-2-[[4-(aminosulfonyl)phenyl]azo]benzoic acid;Rubiazal;mercurousnitrate;3,5-DIAMINO-2-((4-(AMINOSULFONYL)PHENYL)AZO)BENZOIC ACID;SCHEMBL49738;SCHEMBL49739;Sulfachrysoidine [DCF:INN];SULFACHRYSOIDINE [MI];SULFACHRYSOIDINE [INN];CHEMBL2107474;SULFACHRYSOIDINE [MART.];DTXSID00871676;SULFACHRYSOIDINE [WHO-DD];CHEBI:135423;3,5-diamino-2-[p-(sulfamoylphenyl)azo]benzoic acid;Q27256916;Benzoic acid, 3,5-diamino-2-((4-(aminosulfonyl)phenyl)azo)-

Chemical Property of Sulfachrysoidine

Chemical Property:

• Vapor Pressure: 1.37E-21mmHg at 25°C
• Melting Point: above 300°
• Boiling Point: 717.2°Cat760mmHg
• PKA: 3.73±0.36(Predicted)
• Flash Point: 387.6°C
• PSA: 182.60000
• Density: 1.68g/cm³
• LogP: 4.55550
• XLogP3: 0.4
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 4
• Exact Mass: 335.06882509
• Heavy Atom Count: 23
• Complexity: 553

Purity/Quality:

99% ^*data from raw suppliers

SULFACHRYSOIDINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1N=NC2=C(C=C(C=C2N)N)C(=O)O)S(=O)(=O)N

Technology Process of Sulfachrysoidine

There total 1 articles about Sulfachrysoidine 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:

4-Sulfamoyl-benzenediazonium (14289-29-3) + 3.5-diaminobenzoic acid (535-87-5) → sulfachrysoidine (485-41-6)

Guidance literature:

Reference yield:

sulfachrysoidine (485-41-6) → sulfanilamide (63-74-1)

Guidance literature:

With α-D-glucose 6-phosphate; phosphate buffer pH 7.4; rat hepatic azoreductase; NADP; In water; at 37 ℃; Rate constant;

DOI:10.1002/jps.2600730206

Reference yield:

sulfachrysoidine (485-41-6) → 6-amino-2-(4-sulfamoyl-phenyl)-2H-benzotriazole-4-carboxylic acid

Guidance literature:

With ammonia; water; copper(II) sulfate;

upstream raw materials:

4-Sulfamoyl-benzenediazonium

3.5-diaminobenzoic acid

Downstream raw materials:

sulfanilamide