867182-05-6

Basic information

• Product Name: N-[phenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide
• Synonyms: N-[phenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide
• CAS NO: 867182-05-6
• Molecular Weight: 275.156
• Mol File: 867182-05-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-[phenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[phenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide(867182-05-6)
• EPA Substance Registry System: N-[phenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide(867182-05-6)

Safety Data

• Hazardous Substances Data: 867182-05-6(Hazardous Substances Data)

Upstream product

• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 87100-32-1 2-[chloro(phenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 108-24-7 acetic anhydride 
• 75-09-2 dichloromethane 

Downstream Products

• 867181-97-3 (+/-)-1-acetamido-1-phenylmethaneboronic acid 
• 588-46-5 N-(phenylmethyl)acetamide 
• 1185842-29-8 N-[phenyl(3-thienyl)methyl]acetamide 
• 69751-37-7 N-[phenyl(3-pyridyl)methyl]acetamide 
• 5267-35-6 N-(diphenylmethyl)acetamide 
• 5267-47-0 N-((4-methoxyphenyl)(phenyl)methyl)acetamide 
• 1185842-27-6 N-[(4-ethoxycarbonylphenyl)(phenyl)methyl]acetamide 
• 5580-52-9 N-[(3-methylphenyl)(phenyl)methyl]acetamide 
• 5267-50-5 N-[(4-methylphenyl)(phenyl)methyl]acetamide 
• 132666-29-6 N-[(2-methylphenyl)(phenyl)methyl]acetamide 
• 186541-36-6 (E)-N-(1,3-diphenylprop-2-en-1-yl)acetamide 
• 1185842-28-7 N-[(4-trifluoromethylphenyl)(phenyl)methyl]acetamide 
• 1185842-31-2 N-[(4-formylphenyl)(phenyl)methyl]acetamide 
• 1185842-30-1 N-[(4-acetylphenyl)(phenyl)methyl]acetamide 

Relevant articles and documents

α-Amidobenzylation of aryl and alkenyl halides via palladium-catalyzed Suzuki-Miyaura coupling with α-(acylamino) benzylboronic esters

The Suzuki-Miyaura coupling of α-(acetylamino)benzylboronic esters with aryl and alkenyl halides has been achieved using a Pd/P(t-Bu)3 catalyst with KF and H2O in 1,4-dioxane, giving α-substituted benzylamines in high yields. Copyright