Benzamide, 2,2'-dithiobis-

Base Information Edit

Chemical Name:Benzamide, 2,2'-dithiobis-
CAS No.:2527-57-3
Molecular Formula:C14H12 N2 O2 S2
Molecular Weight:304.393
Hs Code.:
European Community (EC) Number:219-766-4
UNII:9X53S9RZ6B
DSSTox Substance ID:DTXSID8062494
Nikkaji Number:J76.664J
Wikidata:Q27273338
ChEMBL ID:CHEMBL50699
Mol file:2527-57-3.mol

Synonyms:3-methyl-2-(3-oxo-3H-benz(d)isothiazol-2-yl)pentanoic acid;CMBB-BIT;N-(1-carboxy-2-methylbutyl)benzisothiazolone;PD 161374;PD-161374

Suppliers and Price of Benzamide, 2,2'-dithiobis-

Supply Marketing:Edit

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

Total 10 raw suppliers

Chemical Property of Benzamide, 2,2'-dithiobis- Edit

Chemical Property:

Melting Point:241-242 °C(Solv: acetic acid (64-19-7))
Boiling Point:517.2°Cat760mmHg
PKA:15.23±0.50(Predicted)
Flash Point:266.6°C
PSA：138.76000
Density:1.43g/cm³
LogP:4.45220
XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:304.03401998
Heavy Atom Count:20
Complexity:331

Purity/Quality:: 99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)N)SSC2=CC=CC=C2C(=O)N
Use Description 2,2'-dithiobisbenzamide, a chemical compound, has applications in various fields. In the field of biochemistry and molecular biology, it serves as a cross-linking reagent for the study of protein-protein interactions and protein structure. Its unique chemical structure allows it to form covalent bonds between sulfhydryl groups in proteins, facilitating the investigation of protein complexes and structural analysis. This compound plays a crucial role in advancing our understanding of biological processes and molecular interactions at the cellular level. Additionally, in organic synthesis, it can be employed as a versatile building block for the creation of specialized organic compounds, contributing to the development of diverse organic molecules with potential applications in pharmaceuticals, materials science, and other industries. Its significance varies within these fields, but it consistently plays a pivotal role in advancing protein research, chemical synthesis, and materials innovation across diverse scientific and industrial applications.

Technology Process of Benzamide, 2,2'-dithiobis-

There total 15 articles about Benzamide, 2,2'-dithiobis- 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: 90.7%

: 4001-73-4
2-Bromobenzamide

: 2527-57-3
2,2'-dithiobisbenzamide

Guidance literature:: With copper(l) iodide; ammonium oxalate; potassium sulfide; In 5,5-dimethyl-1,3-cyclohexadiene; at 60 - 140 ℃; for 8h; Reagent/catalyst; Temperature; Solvent;