81134-67-0

Basic information

• Product Name: Stannane, 1-naphthalenyltriphenyl-
• CAS NO: 81134-67-0
• Molecular Formula: C28H22Sn
• Molecular Weight: 477.193
• Mol File: 81134-67-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Stannane, 1-naphthalenyltriphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Stannane, 1-naphthalenyltriphenyl-(81134-67-0)
• EPA Substance Registry System: Stannane, 1-naphthalenyltriphenyl-(81134-67-0)

Safety Data

• Hazardous Substances Data: 81134-67-0(Hazardous Substances Data)

Upstream product

• 892-20-6 triphenylstannane 
• 90-13-1 1-Chloronaphthalene 
• 108343-70-0 1-naphthyltin trichloride 
• 639-58-7 triphenyltin chloride 
• 703-55-9 1-naphthylmagnesiumbromide 
• 15807-28-0 triphenyl(p-tolyl)tin 
• 33650-14-5 diethyl naphthalen-1-yl phosphate 
• 90-11-9 1-Bromonaphthalene 

Downstream Products

• 2179-93-3 triphenyltin cyanide 
• 962-89-0 triphenyltin bromide 
• 4713-59-1 diphenyltin(IV) dibromide 
• 1954-34-3 triphenyltin isothiocyanate 
• 894-09-7 iodotriphenylstannane 
• 14532-06-0 diphenyltin diiodide 
• 1135-99-5 diphenyltin(IV) dichloride 

Relevant articles and documents

Two-step synthesis of arylstannanes from phenols

The reactions of a number of aryl diethyl phosphates (ArDEP) with (triphenylstannyl)sodium and (trimethylstannyl) sodium in liquid ammonia were studied. Results indicate that the conversion of phenols into the corresponding aryl diethyl phosphates followed by the S displacement with organotin anions is an excellent and convenient method for the synthesis of arylstannanes.

Reactions of Tin-Naphthyl Bond with Halogens and Pseudohalogens

Reactivity of Sn-phenyl or Sn-naphthyl bond in tetraorganotins, PhnSnNp4-n (Ph = phenyl, Np = α-naphthyl; n = 2,3) towards halogens (Br2 and I2), interhalogens (IBr and ICl), interpseudohalogens (BrCN and ICN) and pseudohalogen (SCN)2 has been studied.It is found that the Sn-Np bond is preferentially cleaved yielding in most cases phenyltin derivatives along with the corresponding α-naphthyl halides.