88048-84-4

Basic information

• Product Name: Benzaldehyde, 2-(phenylseleno)-
• CAS NO: 88048-84-4
• Molecular Formula: C13H10OSe
• Molecular Weight: 261.182
• Mol File: 88048-84-4.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(phenylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(phenylseleno)-(88048-84-4)
• EPA Substance Registry System: Benzaldehyde, 2-(phenylseleno)-(88048-84-4)

Safety Data

• Hazardous Substances Data: 88048-84-4(Hazardous Substances Data)

Upstream product

• 23974-72-3 sodium phenylselenide 
• 89-98-5 2-chloro-benzaldehyde 
• 864512-14-1 2-iodophenyl 4-chlorobenzenesulfonate 
• 645-96-5 Benzeneselenol 
• 68-12-2 N,N-dimethyl-formamide 
• 1666-13-3 diphenyl diselenide 
• 6630-33-7 ortho-bromobenzaldehyde 
• 5440-69-7 N-isopropylbenzamide 
• 100-52-7 benzaldehyde 
• 26260-02-6 2-iodobenzaldehyde 
• 40138-16-7 2-formylbenzene boronic acid 
• 591-51-5 phenyllithium 
• 128750-60-7 1-chloro-1-phenyl-3H-2,1-benzoxaselenole 

Downstream Products

• 88048-87-7 2-(phenylseleno)phenylpentadeuteriophenylmethanol 
• 88048-85-5 phenyl[o-(phenylseleno)phenyl]methanol 
• 261-40-5 9H-selenoxanthene 
• 4734-58-1 selenoxanthen-9-one 
• 25562-73-6 2-(hydroxymethyl)phenyl phenyl selenide 
• 128750-59-4 mesitylmethanol 
• 25562-42-9 2-(phenylselanyl)benzoic acid 
• 1421765-47-0 2-(phenylselenyl)phenyldi-2-pyrrolmethane 
• 1421768-87-7 C₂₁H₁₅BF₂N₂OSe 
• 1421768-85-5 C₂₁H₁₅BF₂N₂Se 
• 128750-62-9 1-chloro-3-mesityl-1-phenyl-3H-2,1-benzoxaselenole 
• 128750-61-8 1-chloro-1,3-diphenyl-3H-2,`1-benzoxaselenole 
• 128750-60-7 1-chloro-1-phenyl-3H-2,1-benzoxaselenole 
• 128750-70-9 1-hydroxy-1-phenyl-3H-2,1-benzoxaselenole 

Relevant articles and documents

A new synthesis of highly active Rh-Co alloy nanoparticles supported on N-doped porous carbon for catalytic C-Se cross-coupling and p -nitrophenol hydrogenation reactions

Bimetallic Rh-Co nanoparticles supported on nitrogen-doped porous carbon (Rh-Co/NPC) were synthesized from metal precursors and urea through a simple thermal decomposition/reduction under a nitrogen flow. The Rh-Co/NPC nanocatalyst which contains highly dispersed alloy nanoparticles (～6 nm) showed high catalytic performance as well as good recyclability for the C-Se coupling reaction of diphenyl diselenide and aryl boronic acid and p-nitrophenol reduction.

Palladium-Catalyzed Direct Ortho-C-H Selenylation of Benzaldehydes Using Benzidine as a Transient Directing Group

Benzidine was found to be a novel transient directing group to enable Pd-catalyzed direct selenylation of inert C(sp2)-H bonds of benzaldehydes. Diverse diarylselenides were readily constructed in high efficiency and satisfactory yields with go

METHOD OF PREPARING CORE-SHELL COPPER NANOPARTICLES IMMOBILIZED ON ACTIVATED CARBON AND METHOD OF PREPARING CHALCOGENIDE COMPOUND USING NANOPARTICLES AS CATALYST

Disclosed herein is a method of preparing a Cu/Cu2O core-shell copper nanoparticle catalyst having high catalytic activity from [Cu3(BTC)2] and NaBH4 via a simple chemical reduction method. Also disclosed is a method of preparing a chalcogenide compound by using the nanoparticle catalyst as a heterogeneous catalyst in a cross-coupling reaction between a chalcogenide precursor compound and a boron-containing compound. The disclosed cross-coupling reaction is performed via a simple process, and the disclosed nanoparticle catalyst is compatible with various substrates under mild reaction conditions and exhibits excellent recyclability without a reduction in catalytic activity.