945-77-7

Basic information

• Product Name: Stannane, trimethyl-2-naphthalenyl-
• Synonyms: β-naphthyltrimethylstannane;Trimethyl2-naphthylstannane;Trimethyl(2-naphthyl)stannane;2-(Trimethylstannyl)naphthalene;Stannane, trimethyl-2-naphthalenyl-
• CAS NO: 945-77-7
• Molecular Formula: C₁₃H₁₆Sn
• Molecular Weight: 290.98
• Mol File: 945-77-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Stannane, trimethyl-2-naphthalenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Stannane, trimethyl-2-naphthalenyl-(945-77-7)
• EPA Substance Registry System: Stannane, trimethyl-2-naphthalenyl-(945-77-7)

Safety Data

• Hazardous Substances Data: 945-77-7(Hazardous Substances Data)

Upstream product

• 1336-21-6 ammonium hydroxide 
• 580-13-2 2-bromonaphthalene 
• 1066-45-1 trimethyltin(IV)chloride 
• 594-19-4 tert.-butyl lithium 
• 16519-26-9 diethyl naphthalen-2-yl phosphate 
• 4541-70-2 2-naphthyllithium 
• 91-59-8 naphthalen-2-ylamine 
• 661-69-8 hexamethyldistannane 
• 2243-83-6 2-naphthaloyl chloride 
• 37827-83-1 naphthalene-2-carbonyl fluoride 

Downstream Products

• 10404-26-9 cyclohexyl(naphthalen-2-yl)methanone 
• 1576-47-2 2-naphthalenesulphonamide 
• 179821-61-5 2-Methyl-2-(4-naphth-2-yl-phenyl)morpholine 

Relevant articles and documents

Multifunctional Crown-5-calix[4]arene-based Phase-Transfer Catalysts for Aromatic 18F-Fluorination

Methylated bis-triethylene glycolic crown-5-calix[4]arene (M-BTC5A) as a phase-transfer catalyst showed the best performance among other analogues and even conventional Kryptofix 222 in the nucleophilic aromatic 18F-fluorination of diaryliodonium tosylate precursors owing to (i) the efficient release of reactive "naked"[18F]fluoride, (ii) the high stabilization of the precursor in the reaction, and, presumably, (iii) the ease of access between the precursor and the K18F/M-BTC5A complex facilitated by π-πinteractions. [18F]Flumazenil was produced in high radiochemical yield using M-BTC5A.

Visible-Light-Driven Synthesis of Arylstannanes from Arylazo Sulfones

The visible-light-driven preparation of (hetero)aryl stannanes was carried out under both photocatalyst- and metal-free conditions via irradiation of arylazo sulfones in the presence of hexaalkyldistannanes. The reaction shows a high efficiency and a wide substrates scope. The resulting crude organotin derivatives can be directly employed in a Stille protocol.

Polyarylcarbamoylaza- and -carbamoylalkanedioic acids

This invention relates to a class of novel dicarboxy amide derivatives of lipophilic amines which exhibit squalene synthase inhibition properties. More specifically the compounds are bis-aryl and/or heteroaryl alkyl or cycloalkylamino dicarboxy amides. Co