28096-87-9

Basic information

• Product Name: 2,2'-diaminostilbene
• Synonyms: 2,2'-diaminostilbene
• CAS NO: 28096-87-9
• Molecular Weight: 210.279
• Mol File: 28096-87-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,2'-diaminostilbene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-diaminostilbene(28096-87-9)
• EPA Substance Registry System: 2,2'-diaminostilbene(28096-87-9)

Safety Data

• Hazardous Substances Data: 28096-87-9(Hazardous Substances Data)

Upstream product

• 42467-39-0 2,2'-dinitrostilbene 
• 201230-82-2 carbon monoxide 
• 42467-40-3 2,2'-dinitrostilbene 
• 14275-61-7 (E)-1,2-bis(tri-n-butylstannyl)ethene 
• 615-36-1 2-bromoaniline 
• 25407-11-8 1,2-bis(2-nitrophenyl)ethyne 
• 552-89-6 2-nitro-benzaldehyde 
• 6275-02-1 1,2-bis(o-nitrophenyl)ethylene 
• 23308-83-0 (2-nitrobenzyl)triphenylphosphonium bromide 

Downstream Products

• 120-72-9 indole 
• 62-53-3 aniline 
• 1000205-57-1 C₄₄H₅₈N₂O₄S₂ 
• 1000205-54-8 C₁₆H₁₈N₂O₄S₂ 
• 1000205-55-9 (E)-N,N'-[2,2'-(ethene-1,2-diyl)bis(2,1-phenylene)]dibenzenesulfonamide 
• 1000205-53-7 C₂₈H₂₆N₂O₄S₂ 
• 1000205-56-0 C₂₆H₂₀N₄O₈S₂ 
• 27559-92-8 2,2'-Bis-(o-tolylethinyl)-trans-stilben 
• 34124-14-6 2,2'-ethylenedianiline 
• 27686-42-6 trans-bis(o-iodophenyl)ethylene 

Relevant articles and documents

Intramolecular oxidative diamination and aminohydroxylation of olefins under metal-free conditions

A metal-free procedure that is simple to operate and convenient to handle was developed for the facile intramolecular oxidative diamination of olefins using an iodobenzene diacetate oxidant and a halide additive to furnish bisindolines at room temperature. The present reaction is featured by mild conditions, a broad substrate scope, and excellent functional group tolerance. The same protocol was successfully extended to the aminohydroxylation.

Advancing palladium-catalyzed C-N bond formation: Bisindoline construction from successive amide transfer to internal alkenes

The sequential transfer of two sulfonamides to internal alkenes affords the construction of vicinal diamines. In the presence of a palladium catalyst, the reaction proceeds through two mechanistically different C-N bond formation reactions. It is initiate