1613376-54-7

Basic information

• Product Name: tert-butyl (naphthalen-2-yl(phenyl)methyl)carbonate
• Synonyms: tert-butyl (naphthalen-2-yl(phenyl)methyl)carbonate
• CAS NO: 1613376-54-7
• Molecular Weight: 334.415
• Mol File: 1613376-54-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl (naphthalen-2-yl(phenyl)methyl)carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (naphthalen-2-yl(phenyl)methyl)carbonate(1613376-54-7)
• EPA Substance Registry System: tert-butyl (naphthalen-2-yl(phenyl)methyl)carbonate(1613376-54-7)

Safety Data

• Hazardous Substances Data: 1613376-54-7(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 35060-38-9 (2-naphthyl)phenylmethanol 
• 66-99-9 β-naphthaldehyde 
• 108-86-1 bromobenzene 

Downstream Products

• 1613376-55-8 2-[naphthalen-2-yl(phenyl)methyl]benzo[d]oxazole 
• 1613376-84-3 2-[naphthalen-2-yl(phenyl)methyl]-5-phenyloxazole 
• 1613376-85-4 5-(4-methylphenyl)-2-[naphthalen-2-yl(phenyl)methyl]oxazole 
• 1613376-86-5 5-(4-methoxyphenyl)-2-[naphthalen-2-yl(phenyl)methyl]oxazole 
• 1613376-87-6 C₂₈H₂₃NO₃ 
• 1613376-88-7 2-[naphthalen-2-yl(phenyl)methyl]-5-[4-(trifluoromethyl)phenyl]oxazole 
• 1613376-89-8 5-(4-chlorophenyl)-2-[naphthalen-2-yl(phenyl)methyl]oxazole 
• 1613376-90-1 5-(naphthalen-1-yl)-2-[naphthalen-2-yl(phenyl)methyl]oxazole 
• 1613376-91-2 (E)-2-[naphthalen-2-yl(phenyl)methyl]-5-styryloxazole 
• 1233537-00-2 2-(1-phenylbut-3-en-1-yl)naphthalene 
• 144037-95-6 2-(naphthalen-2-yl)-2-phenylacetonitrile 
• 1136167-10-6 2-naphthyl(phenyl)methyl p-tolyl sulfone 

Relevant articles and documents

Synthesis of triarylmethanes by palladium-catalyzed c-h/c-o coupling of oxazoles and diarylmethanol derivatives

A PdCl2(MeCN)2/PPhCy2 catalyst couples oxazoles with diarylmethyl carbonates or pivalates to form the corresponding triarylmethanes in good yields. The catalysis involves successive secondary benzylic sp3 C-O and heteroaromatic sp2 C-H cleavages and provides an effective access to heteroarene-containing triarylmethanes from nonhalogenated and nonmetalated starting materials, which is complementary to precedented cross-coupling technologies with organic halides and organometallic reagents.