444144-86-9

Basic information

• Product Name: Benzene, 1-chloro-4-(2-nitro-1-phenylethyl)-
• CAS NO: 444144-86-9
• Molecular Formula: C14H12ClNO2
• Molecular Weight: 261.708
• Mol File: 444144-86-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-(2-nitro-1-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-(2-nitro-1-phenylethyl)-(444144-86-9)
• EPA Substance Registry System: Benzene, 1-chloro-4-(2-nitro-1-phenylethyl)-(444144-86-9)

Safety Data

• Hazardous Substances Data: 444144-86-9(Hazardous Substances Data)

Upstream product

• 101671-01-6 1-nitro-2-(4-chlorophenyl)ethylene 
• 595-90-4 tetraphenyltin(IV) 
• 102-96-5 (2-nitroethenyl)benzene 
• 1679-18-1 4-Chlorophenylboronic acid 
• 706-07-0 1-chloro-4-(2-nitrovinyl)benzene 
• 98-80-6 phenylboronic acid 
• 143-66-8 sodium tetraphenyl borate 
• 5153-67-3 nitrostyrene 
• 21700-74-3 (p-chlorophenyl)triethoxysilane 
• 15799-48-1 tetra(p-chlorophenyl)tin 
• 141377-54-0 2-nitro-1-phenylethan-1-ol 
• 108-90-7 chlorobenzene 

Downstream Products

• 6578-33-2 2-(4-chloro-phenyl)-2-phenyl-ethylamine 

Relevant articles and documents

Boosting Conjugate Addition to Nitroolefins Using Lithium Tetraorganozincates: Synthetic Strategies and Structural Insights

We report the first transition metal catalyst- and ligand-free conjugate addition of lithium tetraorganozincates (R4ZnLi2) to nitroolefins. Displaying enhanced nucleophilicity combined with unique chemoselectivity and functional group tolerance, homoleptic aliphatic and aromatic R4ZnLi2 provide access to valuable nitroalkanes in up to 98 % yield under mild conditions (0 °C) and short reaction time (30 min). This is particularly remarkable when employing β-nitroacrylates and β-nitroenones, where despite the presence of other electrophilic groups, selective 1,4 addition to the C=C is preferred. Structural and spectroscopic studies confirmed the formation of tetraorganozincate species in solution, the nature of which has been a long debated issue, and allowed to unveil the key role played by donor additives on the aggregation and structure of these reagents. Thus, while chelating N,N,N’,N’-tetramethylethylenediamine (TMEDA) and (R,R)-N,N,N’,N’-tetramethyl-1,2-diaminocyclohexane (TMCDA) favour the formation of contacted-ion pair zincates, macrocyclic Lewis donor 12-crown-4 triggers an immediate disproportionation process of Et4ZnLi2 into equimolar amounts of solvent-separated Et3ZnLi and EtLi.

Synthesis of palladium nanoparticles using triazolium based ionic liquids: A reusable catalyst for addition of arylboronic acids to nitrostyrenes

Formation of stable and small-sized palladium nanoparticles of diameter 9.4 nm was accomplished by a simple heating of Pd(OAc)2 in 1-octyl-1,2,4-triazolium trifluoroacetate ionic liquid under standard atmospheric hydrogen pressure. Palladium na

Palladium(II)-catalyzed Michael-type hydroarylation of nitroalkenes using aryltins and sodium tetraarylborates

A variety of aryltin compounds and sodium tetraarylborates can be employed for Michael-type hydroarylation reactions of nitroalkenes to afford β-arylnitroalkanes in moderate to good yields in the presence of either LiCl, MgCl2, or CaCl2 and a catalytic amount of palladium(II) salt (0.05 molar amount) in acetic acid. Results show that 50-70% of aryl groups out of all in these aryl compounds can be transferred to the products in this hydroarylation. The addition of a catalytic amount (0.05-0.10 molar amount) of a Lewis acid chloride, BiCl3 or SbCl3, much improves the product yield in some cases.