308366-28-1

Basic information

• Product Name: 2-[12-bromotricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole
• Synonyms: 2-[12-bromotricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole
• CAS NO: 308366-28-1
• Molecular Formula: C₂₁H₂₂BrNO
• Molecular Weight: 384.30948
• Mol File: 308366-28-1.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[12-bromotricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[12-bromotricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole(308366-28-1)
• EPA Substance Registry System: 2-[12-bromotricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole(308366-28-1)

Safety Data

• Hazardous Substances Data: 308366-28-1(Hazardous Substances Data)

Upstream product

• 308366-29-2 N-(1-hydroxy-2-methyl-2-propyl)[2.2]paracyclophane-13-carboxamide 
• 108869-37-0 [2.2]paracyclophane-4-carboxylic acid chloride 
• 1908-61-8 4-bromo[2.2]paracyclophane 
• 1633-22-3 [2.2]Paracyclophan 
• 20586-49-6 [2.2]paracyclophane-4-carboxylic acid 
• 56439-07-7 pseudo-meta-bromo-<2.2>paracyclophane-4-carboxylic acid 
• 308366-27-0 (4Sp,13Rp)-4-bromo-N-(1-hydroxy-2-methylprop-2-yl)[2.2]paracyclophane-13-carboxamide 
• 308366-30-5 4-(4,4-dimethyloxazolin-2-yl)[2.2]paracyclophane 

Downstream Products

• 308366-30-5 4-(4,4-dimethyloxazolin-2-yl)[2.2]paracyclophane 
• 308366-33-8 4-phenylthio-13-(4,4-dimethyloxazolin-2-yl)[2.2]paracyclophane 

Relevant articles and documents

Regulation of the flexibility of planar chiral [2.2]paracyclophane ligands and its significant impact on enantioselectivity in asymmetric reactions of diethylzinc with carbonyl compounds

A series of planar chiral ligands derived from [2.2]paracyclophane were synthesized and applied as catalysts in enantioselective additions of diethylzinc to aldehydes and α,β-unsaturated ketones. When ligand 10 with a dimethyl hydroxymethyl as the substituent was used, the enantioselectivity of the reaction of diethylzinc with aldehydes was much higher than when using ligand 3c with diphenyl hydroxymethyl as the substituent. The situation was the same with the 1,4-addition of diethylzinc to α,β-unsaturated ketones with 63-83% ee being obtained when the hydroxymethyl substituted ligand 7b was used, while almost no enantioselectivity was afforded if ligand 3c was used. The role of planar chirality is also studied.