Benzenamine, 2,2'-dithiobis[4-nitro-

Base Information

• Chemical Name: Benzenamine, 2,2'-dithiobis[4-nitro-
• CAS No.: 58381-87-6
• Molecular Formula: C12H10N4O4S2
• Molecular Weight: 338.368
• DSSTox Substance ID: DTXSID40396530
• Nikkaji Number: J1.458.296G
• Wikidata: Q82197293

Synonyms:58381-87-6;Benzenamine, 2,2'-dithiobis[4-nitro-;2,2'-disulfanediylbis(4-nitroaniline);2-[(2-amino-5-nitrophenyl)disulfanyl]-4-nitroaniline;SCHEMBL8576404;DTXSID40396530;2,2'-Dithiobis(4-nitroaniline)

Chemical Property of Benzenamine, 2,2'-dithiobis[4-nitro-

Chemical Property:

• PSA: 194.28000
• LogP: 5.67560
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 3
• Exact Mass: 338.01434716
• Heavy Atom Count: 22
• Complexity: 379

Purity/Quality:

99% ^*data from raw suppliers

2,2'-Disulfanediylbis(4-nitroaniline) 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1[N+](=O)[O-])SSC2=C(C=CC(=C2)[N+](=O)[O-])N)N

Technology Process of Benzenamine, 2,2'-dithiobis[4-nitro-

There total 2 articles about Benzenamine, 2,2'-dithiobis[4-nitro- 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: 97.0%

6-nitrobenzo[d]thiazole (2942-06-5) → 2-[(2-amino-5-nitrophenyl)dithio]-4-nitrophenylamine (58381-87-6)

Guidance literature:

6-nitrobenzo[d]thiazole; With ethylenediamine; In glycerol; at 90 ℃; for 0.166667h; Inert atmosphere;

With dihydrogen peroxide; In glycerol; at 5 ℃; for 0.5h; Inert atmosphere;

DOI:10.1016/j.bioorg.2019.103537

Reference yield:

→ 2-[(2-amino-5-nitrophenyl)dithio]-4-nitrophenylamine (58381-87-6)

Guidance literature:

6-Nitrobenzothiazol, 1) NaOCH3, 2) Br2;

Reference yield: 91.0%

2-[(2-amino-5-nitrophenyl)dithio]-4-nitrophenylamine (58381-87-6) + 3,4-dimethoxy-benzaldehyde (120-14-9) → 2-(3,4-dimethoxyphenyl)-6-nitrobenzothiazole (1336853-75-8)

Guidance literature:

With sodium metabisulfite; In dimethyl sulfoxide; at 120 ℃;

DOI:10.1016/j.tet.2011.08.004

upstream raw materials:

6-nitrobenzo[d]thiazole

Downstream raw materials:

6-nitro-benzo[1,2,3]thiadiazole

6-bromo-benzo[1,2,3]thiadiazole

benzo[d][1,2,3]thiadiazol-6-amine

6-chloro-1,2,3-benzothiadiazole

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