14338-21-7

Basic information

• Product Name: Aluminum, tris(4-methylphenyl)-
• CAS NO: 14338-21-7
• Molecular Formula: C21H21Al
• Molecular Weight: 300.379
• Mol File: 14338-21-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Aluminum, tris(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Aluminum, tris(4-methylphenyl)-(14338-21-7)
• EPA Substance Registry System: Aluminum, tris(4-methylphenyl)-(14338-21-7)

Safety Data

• Hazardous Substances Data: 14338-21-7(Hazardous Substances Data)

Upstream product

• 7446-70-0 aluminum (III) chloride 
• 624-31-7 4-tolyl iodide 
• 106-38-7 para-bromotoluene 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 100-58-3 phenylmagnesium bromide 
• 537-64-4 bis(p-tolyl)mercury 

Downstream Products

• 5440-76-6 (4-methylphenyl)diphenylmethanol 
• 99-94-5 p-Toluic acid 
• 1517-63-1 4-methylphenyl(phenyl)methanol 
• 16112-21-3 2-(4-methylphenyl)-1,3-benzothiazole 
• 17286-62-3 2-(4-methylphenyl)quinoxaline 
• 16107-82-7 4-(4-methylphenyl)-2-phenyl-quinazoline 
• 1335558-23-0 7-chloro-4-(4-methylphenyl)quinoline 
• 4714-21-0 E-1-methyl-4-styryl-benzene 
• 1657-45-0 (Z)-4-methylstilbene 
• 50670-50-3 p-(p-tolyl)benzonitrile 
• 1202574-24-0 2-chloro-4-(4-methylphenyl)pyridine 
• 4467-06-5 2-(4-methylphenyl)pyridine 
• 27331-34-6 1-(4-methylphenyl)naphthalene 
• 1002328-13-3 (S)-(1-naphthyl)-(4'-methylphenyl)methanol 

Relevant articles and documents

The inexpensive additive N-methylmorpholine effectively decreases the equivalents of nucleophiles in the catalytic highly enantioselective arylation of aryl aldehydes

Highly enantioselective arylation of aryl aldehydes catalyzed by (S)-H8-BINOL-Ti(Oi-Pr)2 complex in the presence of N-methylmorpholine (NMM) as an effective and inexpensive additive is described for the first time. We found high enan

Sequential [3,3]-Sigmatropic Rearrangement/Nucleophilic Arylation of N -(Benzoyloxy)enamides towards the Preparation of Cyclic β-Aryl-β-amino Alcohols

A new method has been developed for the efficient synthesis of cyclic β-aryl-β-amino alcohol derivatives bearing a tetrasubstituted carbon center via the [3,3]-sigmatropic rearrangement of N-(benzoyl oxy)enamides followed by nucleophilic arylation reactio

Process for the Preparation of ?-C-Aryl Glucosides

The present invention provides processes for stereoselectively preparing C-arylglucosides that can be useful as synthetic building block or drugs, including SGLT2 inhibitors.