N4-Sulfanilylsulfanilamide

Base Information

Chemical Name:N4-Sulfanilylsulfanilamide
CAS No.:547-52-4
Molecular Formula:C12H13N3O4S2
Molecular Weight:327.385
Hs Code.:2935009090
UNII:HKA2A1D99J
DSSTox Substance ID:DTXSID40871756
Nikkaji Number:J166.101I
Wikidata:Q27279971
Pharos Ligand ID:5UU3BJXHXP6S
ChEMBL ID:CHEMBL269122
Mol file:547-52-4.mol

Synonyms:disulphane

Suppliers and Price of N4-Sulfanilylsulfanilamide

Supply Marketing:

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

Matrix Scientific
4-Amino-N-[4-(aminosulfonyl)phenyl]benzenesulfonamide
1g
$ 316.00

Matrix Scientific
4-Amino-N-[4-(aminosulfonyl)phenyl]benzenesulfonamide
10g
$ 1170.00

Matrix Scientific
4-Amino-N-[4-(aminosulfonyl)phenyl]benzenesulfonamide
5g
$ 810.00

American Custom Chemicals Corporation
N4-SULFANILYLSULFANILAMIDE 95.00%
5MG
$ 503.99

Total 1 raw suppliers

Chemical Property of N4-Sulfanilylsulfanilamide

Chemical Property:

Vapor Pressure:4.26E-14mmHg at 25°C
Melting Point:133-134°
Refractive Index:1.6390 (estimate)
Boiling Point:594.4°C at 760 mmHg
PKA:pKa 3.20(H2O t = 25 I = 0.05) (Uncertain);8.23(H2O t = 25 I = 0.05) (Uncertain)
Flash Point:313.3°C
PSA：149.11000
Density:1.56g/cm³
LogP:4.23310
XLogP3:0.6
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:327.03474825
Heavy Atom Count:21
Complexity:534

Purity/Quality:

98%+ ^*data from raw suppliers

4-Amino-N-[4-(aminosulfonyl)phenyl]benzenesulfonamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N)S(=O)(=O)NC2=CC=C(C=C2)S(=O)(=O)N

Technology Process of N4-Sulfanilylsulfanilamide

There total 9 articles about N4-Sulfanilylsulfanilamide 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:

: 63-74-1
sulfanilamide

: 547-52-4
4-amino-N-[4-(aminosulfonyl)phenyl]-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous acetone; sodium hydrogencarbonate

2: aqueous hydrochloric acid

With hydrogenchloride; sodium hydrogencarbonate; acetone;
DOI:10.1021/ja01872a020

Reference yield:

: 5702-84-1
N-(N-acetyl-sulfanilyl)-sulfanilic acid amide

: 547-52-4
4-amino-N-[4-(aminosulfonyl)phenyl]-benzenesulfonamide

Guidance literature:: With hydrogenchloride;
DOI:10.1021/ja01872a020

Reference yield:

: 121-60-8
p-acetylaminobenzenesulfonyl chloride

: 547-52-4
4-amino-N-[4-(aminosulfonyl)phenyl]-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous acetone; sodium hydrogencarbonate

2: aqueous hydrochloric acid

With hydrogenchloride; sodium hydrogencarbonate; acetone;
DOI:10.1021/ja01872a020