100-32-3 | 4,4'-Dinitrodiphenyl disulfide

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$14.00	$10.00
10g	95%	in stock	$15.00	$11.00
100g	95%	in stock	$120.00	$84.00
500g	95%	in stock	$441.00	$309.00

Description

• Catalog Number: AA00036
• Chemical Name: 4,4'-Dinitrodiphenyl disulfide
• CAS Number: 100-32-3
• Molecular Formula: C12H8N2O4S2
• Molecular Weight: 308.3329
• MDL Number: MFCD00003573
• SMILES: [O-][N+](=O)c1ccc(cc1)SSc1ccc(cc1)[N+](=O)[O-]

Computed Properties

• Complexity: 308
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• XLogP3: 3.7

Upstream Synthesis Route

Disulfide, bis(4-nitrophenyl) is a versatile compound commonly used in chemical synthesis as a powerful oxidizing agent and a key building block in organic reactions. Its unique properties make it an essential tool for researchers and chemists in a wide range of applications. In particular, this compound is widely employed in the synthesis of various organic compounds, including pharmaceuticals, dyes, and polymers. Its ability to facilitate oxidation reactions makes it indispensable in the creation of complex molecules and the modification of existing compounds. By leveraging the reactivity of disulfide, bis(4-nitrophenyl), chemists can efficiently and effectively carry out a diverse array of chemical transformations, enabling the development of novel materials and compounds for various industries.

Literature

• Sulfur-substituted tetrahedranes.

  Journal of the American Chemical Society 20110803

• Photooxidative coupling of thiophenol derivatives to disulfides.

  The journal of physical chemistry. A 20101118

• 4-Amino-phenyl-sulfur penta-fluoride.

  Acta crystallographica. Section E, Structure reports online 20080201

• Zinc protects HeLa-tat cells against free radical cytotoxicity induced by glucose.

  Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) 20050101

• The role of nonbonded sulfur-oxygen interaction in the dissociative electron transfer to nitro-substituted arenesulfenyl chlorides.

  Journal of the American Chemical Society 20040707

• 2-Nitrophenyl 4-nitrophenyl disulfide.

  Acta crystallographica. Section C, Crystal structure communications 20020801

• Evaluation of selected chemotypes in coupled cellular and molecular target-based screens identifies novel HIV-1 zinc finger inhibitors.

  Journal of medicinal chemistry 19960913