Molecular Biology Reagents

1,8-Diazabicyclo[5.4.0]undec-7-ene is a bicyclic amidine base. It is non-nucleophilic, sterically hindered, tertiary amine base in organic chemistry. It is reported to be superior to amine catalyst in Baylis-Hillman reaction. It promotes the

1,8-Diazabicyclo[5.4.0]undec-7-ene is a bicyclic amidine base. It is non-nucleophilic, sterically hindered, tertiary amine base in organic chemistry. It is reported to be superior to amine catalyst in Baylis-Hillman reaction. It promotes the

1,8-Diazabicyclo[5.4.0]undec-7-ene is a bicyclic amidine base. It is non-nucleophilic, sterically hindered, tertiary amine base in organic chemistry. It is reported to be superior to amine catalyst in Baylis-Hillman reaction. It promotes the

1,8-Diazabicyclo[5.4.0]undec-7-ene is a bicyclic amidine base. It is non-nucleophilic, sterically hindered, tertiary amine base in organic chemistry. It is reported to be superior to amine catalyst in Baylis-Hillman reaction. It promotes the

Hill Formula: C₉H₁₆N₂ CAS Number: 6674-22-2 UN Number: UN2922

Hill Formula: C₉H₁₆N₂ CAS Number: 6674-22-2 UN Number: UN2922

Hill Formula: C₉H₁₆N₂ CAS Number: 6674-22-2 UN Number: UN2922

DescriptionPolymerization catalyst.

Description1,8-Dimethyl-1,4,8,11-tetraazacyclotetradecane is a heterocyclic building block.1,8-Dimethyl-1,4,8,11-tetraazacyclotetradecane may be used as a precursor for the synthesis of `trans′-difunctionalized derivatives. It may also be used in

Description1,8-Dimethyl-1,4,8,11-tetraazacyclotetradecane is a heterocyclic building block.1,8-Dimethyl-1,4,8,11-tetraazacyclotetradecane may be used as a precursor for the synthesis of `trans′-difunctionalized derivatives. It may also be used in

1,8-Naphthosultamyl group is a novel PBP2a (penicillin-binding protein 2a)-binding, anti-methicillin-resistant Staphylococcus aureus (MRSA) pharmacophore.

1,8-Naphthosultamyl group is a novel PBP2a (penicillin-binding protein 2a)-binding, anti-methicillin-resistant Staphylococcus aureus (MRSA) pharmacophore.