14409-95-1

Basic information

• Product Name: 1H-Phosphole, 2,5-dihydro-3,4-dimethyl-1-phenyl-
• CAS NO: 14409-95-1
• Molecular Formula: C12H15P
• Molecular Weight: 190.225
• Mol File: 14409-95-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1H-Phosphole, 2,5-dihydro-3,4-dimethyl-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Phosphole, 2,5-dihydro-3,4-dimethyl-1-phenyl-(14409-95-1)
• EPA Substance Registry System: 1H-Phosphole, 2,5-dihydro-3,4-dimethyl-1-phenyl-(14409-95-1)

Safety Data

• Hazardous Substances Data: 14409-95-1(Hazardous Substances Data)

Upstream product

• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 1073-47-8 phenyldibromophosphine 
• 3376-52-1 pentaphenylcyclopentaphosphane 
• 15450-93-8 3-methyl-1-phenyl-3-phospholene 
• 563-79-1 2,3-Dimethyl-2-butene 
• 644-97-3 Dichlorophenylphosphine 
• 638-21-1 phenylphosphane 
• 113132-36-8 bis(cyclopentadienyl)-3,4-dimethyl-3-zirconocene 
• 89865-20-3 (1-Methoxy-1-phenylphosphanyl-ethyl)-dimethyl-amine 
• 28273-33-8 1-bromo-3,4-dimethyl-Δ³-phospholen 
• 75589-83-2 N,N-dimethylamino-P-phenyl-C-methylmethylenephosphine 
• 710-89-4 3,4-dimethyl-1-phenyl-3-phospholene 1-oxide 

Downstream Products

• 333304-10-2 cis-bis-[1-phenyl-3,4-dimethylphospholene]-(pentacarbonyl)tungsten 
• 82281-49-0 [1-phenyl-3,4-dimethylphospholene](pentacarbonyl)tungsten 
• 1173091-15-0 1,4-dimethyl-2-phenyl-1,4,2-diazaphospholidin-3,5-dione 
• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 710-89-4 3,4-dimethyl-1-phenyl-3-phospholene 1-oxide 
• 1173091-16-1 3,4-dimethyl-1-phenyl-2,3-dihydro-1H-phosphole 
• 333304-08-8 [(CH₃)2C₄H₄P(C₆H₅)P(C₆H₅)(W(CO)5)CuCl]2 
• 143924-60-1 3,4-dimethyl-1-supermesityl-3-phospholene 
• 1638-86-4 diethyl phenylphosphonite 
• 23855-82-5 tetraethoxy-phenyl-λ⁵-phosphane 
• 58608-01-8 3,4-dimethyl-1-phenyl-2,5-dihydro-1H-phosphole 1-selenide 
• 39997-45-0 1-phenyl-3,4-dimethylphospholene sulfide 
• 58612-65-0 1-phenyl-3,4-dimethyl-3-phospholene methiodide 
• 40962-33-2 N-(3,4-dimethyl-1-phenyl-phospholan-3-yl)-ethane-1,2-diamine 

Relevant articles and documents

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1,2-Phosphaborines: Hybrid Inorganic/Organic P-B Analogues of Benzene

Photolysis of the cyclic phosphine oligomer [PPh]5 in the presence of pentaarylboroles leads to the formation of 1,2-phosphaborines by the formal insertion of a phenylphosphinidene fragment into the endocyclic C-B bond. The solid-state structur

Metallacycle transfer from zirconium to main group elements: A versatile synthesis of heterocycles

The reaction of zirconium metallacycles is used to produce a variety of main group heterocycles including borole Diels-Alder dimers, galloles, indacyclopentadienes, siloles, germoles, stannoles, phospholes, arsoles, stiboles, bismoles, thiophenes, selenophenes, dihydrothiophenes, dihydroselenophenes, tetrahydrothiophenes, tetrahydro-selenophenes, stannacyclopentanes, phospholenes, and isothiazoles. An X-ray crytallographic study of the borole DielsAlder dimer of 1-phenyl-2,3,4,5-tetramethylborole is discussed and compared with the structure of 7-norbornenyl carbenium ions. The scope and potential for this metallacycle transfer reaction are delineated.