787-64-4

Basic information

• Product Name: TIMTEC-BB SBB006314
• Synonyms: TIMTEC-BB SBB006314;2-(4-Nitrophenyl)benzofuran;2-(4-nitrophenyl)-1-benzofuran
• CAS NO: 787-64-4
• Molecular Formula: C₁₄H₉NO₃
• Molecular Weight: 239.23
• Mol File: 787-64-4.mol
• Article Data: 52

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TIMTEC-BB SBB006314(CAS DataBase Reference)
• NIST Chemistry Reference: TIMTEC-BB SBB006314(787-64-4)
• EPA Substance Registry System: TIMTEC-BB SBB006314(787-64-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 787-64-4(Hazardous Substances Data)

Upstream product

• 17490-72-1 2-(4-nitrobenzyloxy)benzaldehyde 
• 80645-55-2 bromure de p-nitrobenzoyloxy-2 benzyltriphenylphosphonium 
• 98437-24-2 benzofuran-2-boronic acid 
• 586-78-7 para-nitrophenyl bromide 
• 100-01-6 4-nitro-aniline 
• 1060684-38-9 2-(4'-nitrophenylethynyl)-O-triisopropylsilylphenol 
• 1123247-20-0 sodium (2-benzofuryl)dimethylsilanolate 
• 636-98-6 p-nitrobenzene iodide 
• 60981-57-9 (benzofuran-2-yl)trimethylsilane 
• 15959-31-6 sodium 4-nitrobenzenesulfinate 
• 91703-34-3 2-(β,β-dibromovinyl)phenol 
• 271-89-6 1-benzofurane 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 32438-31-6 (2,2-diethoxy-ethoxy)-benzene 

Downstream Products

• 782-18-3 4-(benzofuran-2-yl)benzenamine 
• 1373220-98-4 Br^(1-)*C₂₅H₁₉N₂O₂⁽¹⁺⁾ 
• 1373221-00-1 Br^(1-)*C₂₅H₁₉N₂O₃⁽¹⁺⁾ 
• 1373221-02-3 Br^(1-)*C₂₆H₂₁N₂O₃⁽¹⁺⁾ 
• 1373221-04-5 Br^(1-)*C₂₅H₁₈FN₂O₂⁽¹⁺⁾ 
• 1373221-06-7 Br^(1-)*C₂₅H₁₈BrN₂O₂⁽¹⁺⁾ 
• 1373221-10-3 Br^(1-)*C₃₁H₂₃N₂O₂⁽¹⁺⁾ 
• 1373220-83-7 C₁₇H₁₂N₂O 
• 1373220-86-0 Br^(1-)*C₂₄H₁₉N₂O⁽¹⁺⁾ 
• 1373220-89-3 Br^(1-)*C₂₄H₁₈BrN₂O⁽¹⁺⁾ 
• 1373220-92-8 Br^(1-)*C₂₀H₁₇N₂O⁽¹⁺⁾ 
• 1373220-95-1 C₂₁H₂₁N₂O⁽¹⁺⁾*I^(1-) 
• 101046-17-7 N-<4-(2-benzofuranyl)phenyl>maleamic acid 

Relevant articles and documents

Discovery and computational studies of 2-phenyl-benzoxazole acetamide derivatives as promising P2Y14R antagonists with anti-gout potential

The P2Y14 nucleotide receptor, a subtype of P2Y receptors, is implicated in many human inflammatory diseases. Based on the identification of favorable residues of two screening hits in the almost symmetrical P2Y14 binding domain, we

GC/MSn analysis of the crude reaction mixtures from Friedel–Crafts acylation: Unambiguous identification and differentiation of 3-aroylbenzofurans from their 4- and 6-regioisomers

Rationale: 3-Aroylbenzofurans and their 2-nitrophenyl derivatives constitute fundamental intermediates for the synthesis of target compounds with pharmaceutical properties. However, their preparation via the Friedel–Crafts acylation of 2-phenylbenzofurans

Acid-promoted selective synthesis of trifluoromethylselenolated benzofurans with Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate

A Br?nsted acid-promoted trifluoromethylselenolation of benzofurans was disclosed by using Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate as a stable and easily prepared electrophilic trifluoromethylselenolating reagent. A wide range of SeCF3-substituted benzofuran derivatives were obtained in moderate to good yields with excellent regioselectivity. The tandem cyclization/trifluoromethylselenolation procedure of 1-methoxy-2-(arylethynyl)benzenes were also realized by engaging FeCl3 as the catalyst.