35010-17-4

Basic information

• Product Name: Benzene, 1-nitro-2-(phenylethynyl)-
• CAS NO: 35010-17-4
• Molecular Formula: C14H9NO2
• Molecular Weight: 223.231
• Mol File: 35010-17-4.mol
• Article Data: 103

Chemical Properties

• CAS DataBase Reference: Benzene, 1-nitro-2-(phenylethynyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-nitro-2-(phenylethynyl)-(35010-17-4)
• EPA Substance Registry System: Benzene, 1-nitro-2-(phenylethynyl)-(35010-17-4)

Safety Data

• Hazardous Substances Data: 35010-17-4(Hazardous Substances Data)

Upstream product

• 13146-23-1 copper(I) phenylacetylenide 
• 609-73-4 o-nitroiodobenzene 
• 536-74-3 phenylacetylene 
• 501-65-5 diphenyl acetylene 
• 32584-71-7 diphenyl(phenylethynyl)stibine 
• 126472-97-7 12-phenylethynyl-N-methyl-5,6,7,12-tetrahydrodibenz[c,f][1,5]azastibocine 
• 88-73-3 2-Chloronitrobenzene 
• 591-50-4 iodobenzene 
• 3034-94-4 3-nitrophenylacetylene 
• 2170-06-1 1-Phenyl-2-(trimethylsilyl)acetylene 
• 3958-60-9 2-nitrophenylmethyl bromide 
• 552-16-9 ortho-nitrobenzoic acid 
• 365-33-3 2-nitrobenzenediazonium tetrafluoroborate 
• 637-44-5 phenylpropyolic acid 

Downstream Products

• 1969-74-0 2-phenylisatogen 
• 62058-64-4 (Z)-2-aminostilbene 
• 35010-10-7 1-(2-nitrophenyl)-2-phenylethane-1,2-dione 
• 13141-38-3 2-phenylethynylaniline 
• 5697-85-8 2-(2-phenylethyl)aniline 
• 948-65-2 2-phenyl-indole 
• 104682-98-6 N-(2-(2-phenylethynyl)phenyl)benzamide 
• 53330-45-3 phenyl(2-phenyl-1H-indol-1-yl)methanone 
• 2989-63-1 2-phenyl-3H-indol-3-one 

Relevant articles and documents

Zeolitic imidazolate frameworks-67 (ZIF-67) supported PdCu nanoparticles for enhanced catalytic activity in Sonogashira-Hagihara and nitro group reduction under mild conditions

A bimetallic PdCu supported on amine functionalized ZIF-67 is shown to be efficient catalyst in Sonogashira-Hagihara coupling reaction of aryl iodides at room temperature and aryl bromides at 40 oC. In addition, the catalyst is used in the reduction of 4-

Synthesis of N-Hydroxyindole Derivatives via Pd-Catalyzed Electrophilic Cyclization

-

Catalytic asymmetric formal [3+2] cycloaddition of isatogens with azlactones to construct indolin-3-one derivatives

The chiral amide-guanidine-catalyzed asymmetric formal [3+2] cycloaddition of isatogens with azlactones is presented. This strategy provided a facile and feasible route to chiral indolin-3-one derivatives bearing two contiguous tetrasubstituted stereocent