1155-00-6 | Bis(2-nitrophenyl) disulfide

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$15.00	$10.00
1g	97%	in stock	$16.00	$11.00
5g	97%	in stock	$23.00	$16.00
25g	97%	in stock	$39.00	$27.00
100g	97%	in stock	$145.00	$101.00
500g	97%	in stock	$512.00	$358.00

Description

• Catalog Number: AA20636
• Chemical Name: Bis(2-nitrophenyl) disulfide
• CAS Number: 1155-00-6
• Molecular Formula: C12H8N2O4S2
• Molecular Weight: 308.3329
• MDL Number: MFCD00007130
• SMILES: [O-][N+](=O)c1ccccc1SSc1ccccc1[N+](=O)[O-]

Upstream Synthesis Route

Bis(2-nitrophenyl) disulfide, also known as BNDS, is a versatile compound widely used in chemical synthesis as a cross-linking agent and as a reagent for thiol-disulfide exchange reactions. In organic chemistry, BNDS plays a crucial role in the formation of disulfide bonds between sulfhydryl groups, aiding in the synthesis of various organic compounds and polymers.One common application of BNDS is in peptide synthesis, where it is utilized for the selective protection of cysteine residues to prevent unwanted chemical reactions during peptide assembly. BNDS can be used to temporarily block thiol groups in peptides, allowing for specific modifications to be made before deprotection to yield the final peptide product.Additionally, BNDS is employed in the synthesis of disulfide-containing drugs and pharmaceuticals, where controlled disulfide bond formation is essential for the stability and bioactivity of the final product. By acting as a bridge between sulfhydryl groups, BNDS facilitates the formation of structurally complex molecules with enhanced pharmacological properties.Furthermore, BNDS finds application in materials science for the preparation of disulfide-linked polymers and dendrimers, where controlled cross-linking is crucial for the mechanical strength and thermal stability of the resulting materials. The unique reactivity of BNDS towards thiols makes it a valuable tool in designing novel polymeric architectures with tailored properties for various industrial applications.In conclusion, Bis(2-nitrophenyl) disulfide is a versatile compound with diverse applications in chemical synthesis, particularly in the formation of disulfide bonds for peptide modification, drug synthesis, and polymer engineering. Its selective reactivity towards sulfhydryl groups makes it an indispensable reagent for designing complex molecules and materials with tailored functionalities and properties.