126552-56-5

Basic information

• Product Name: N-[2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-2-chloro-N-(3,4-dimethoxy-phenyl)-2-methylsulfanyl-acetamide
• CAS NO: 126552-56-5
• Molecular Weight: 594.954
• Mol File: 126552-56-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-2-chloro-N-(3,4-dimethoxy-phenyl)-2-methylsulfanyl-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-2-chloro-N-(3,4-dimethoxy-phenyl)-2-methylsulfanyl-acetamide(126552-56-5)
• EPA Substance Registry System: N-[2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-2-chloro-N-(3,4-dimethoxy-phenyl)-2-methylsulfanyl-acetamide(126552-56-5)

Safety Data

• Hazardous Substances Data: 126552-56-5(Hazardous Substances Data)

Upstream product

• 79388-13-9 α-chloro-α-(methylthio)-acetyl chloride 
• 126523-15-7 [2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-(3,4-dimethoxy-phenyl)-amine 
• 64434-31-7 2-bromo-4-benzyloxy-5-methoxyphenylacetic acid 
• 343232-31-5 4-benzyloxy-2-bromo-5-methoxyphenylacetic acid chloride 
• 126523-14-6 2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-N-(3,4-dimethoxy-phenyl)-acetamide 

Downstream Products

• 126523-17-9 1-[2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-5,6-dimethoxy-3-methylsulfanyl-1,3-dihydro-indol-2-one 
• 126523-19-1 1-[2-(4-Hydroxy-3-methoxy-phenyl)-ethyl]-5,6-dimethoxy-1,3-dihydro-indol-2-one 
• 17138-39-5 2-benzyloxy-5,6,12,12a-tetrahydro-3,9,10-trimethoxydibenz[b,g]indolizine 
• 126523-21-5 1-[2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-5,6-dimethoxy-1H-indole 
• 126523-18-0 1-[2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-ethyl]-5,6-dimethoxy-1,3-dihydro-indol-2-one 
• 17389-24-1 (+/-)-O-benzylcryptaustoline 
• 126523-22-6 2,2'-Bis-benzyloxy-3,9,10,3',9',10'-hexamethoxy-5,6,5',6'-tetrahydro-[12,12']bi[indolo[2,1-a]isoquinolinyl] 

Relevant articles and documents

A NOVEL TOTAL SYNTHESIS OF (+/-)-CRYPTAUSTOLINE, A DIBENZOPYRROCOLINE ALKALOID

(+/-)-Cryptaustoline (1), a dibenzopyrrocoline alkaloid, was efficiently synthesized from the readily available N-phenethylaniline (7) via the N-phenethyloxindole (12) or the N-phenethylindole (14) by the Bischler-Napieralski reaction or by radical cycliz