1427179-44-9

Basic information

• Product Name: 2,6-dimethylphenyl 2-phenylbutanoate
• Synonyms: 2,6-dimethylphenyl 2-phenylbutanoate
• CAS NO: 1427179-44-9
• Molecular Weight: 268.356
• Mol File: 1427179-44-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,6-dimethylphenyl 2-phenylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dimethylphenyl 2-phenylbutanoate(1427179-44-9)
• EPA Substance Registry System: 2,6-dimethylphenyl 2-phenylbutanoate(1427179-44-9)

Safety Data

• Hazardous Substances Data: 1427179-44-9(Hazardous Substances Data)

Upstream product

• 576-26-1 2.6-dimethylphenol 
• 90-27-7 2-Phenylbutyric acid 

Downstream Products

• 1427179-72-3 (Z)-1-methyl-2-(3-phenyloct-3-en-4-yl)benzene 
• 1427179-74-5 (E)-(4-methyloct-3-en-3-yl)benzene 
• 1427179-75-6 (Z)-oct-3-ene-3,4-diyldibenzene 
• 1427179-77-8 (Z)-(2-butylpent-2-ene-1,3-diyl)dibenzene 
• 1427179-78-9 (E)-(2-butylpent-2-ene-1,3-diyl)dibenzene 
• 1427179-83-6 (Z)-(1-(o-tolyl)but-1-ene-1,2-diyl)dibenzene 
• 122902-56-1 (E)-(1-(o-tolyl)but-1-ene-1,2-diyl)dibenzene 
• 1427179-84-7 (Z)-(4-butyldec-3-en-3-yl)benzene 
• 1427179-85-8 (Z)-(3-butylhex-3-en-1-yne-1,4-diyl)dibenzene 
• 1427179-56-3 (Z)-1,2-diphenylbut-1-en-1-yl diphenylphosphate 
• 1427179-58-5 (Z)-1-(furan-2-yl)-2-phenylbut-1-en-1-yl diphenylphosphate 
• 1427179-52-9 (Z)-diethyl (3-phenyloct-3-en-4-yl)phosphate 
• 39604-15-4 2,6-dimethylphenyl diethyl phosphate 
• 1427179-55-2 (Z)-2,2-dimethyl-4-phenylhex-3-en-3-yl diethylphosphate 

Relevant articles and documents

Stereoselective synthesis of all-carbon tetrasubstituted alkenes from in situ generated ketenes and organometallic reagents

Stereoselective synthesis of tetrasubstituted alkenes is a challenging problem in chemical synthesis. New protocols to access this important, yet simple, structural motif are of fundamental significance because they are found in many valuable molecules and can be utilized in a variety of important complexity building chemical transformations. The two-step strategy presented herein involves stereoselective generation of an alkenyl pseudohalide followed by a stereospecific metal-catalyzed cross-coupling.