879375-42-5

Basic information

• Product Name: 2-Butenoic acid, 4-[(1H-indol-2-ylmethyl)(phenylmethyl)amino]-3-methyl-, ethyl ester, (2E)-
• CAS NO: 879375-42-5
• Molecular Formula: C23H26N2O2
• Molecular Weight: 362.472
• Mol File: 879375-42-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Butenoic acid, 4-[(1H-indol-2-ylmethyl)(phenylmethyl)amino]-3-methyl-, ethyl ester, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butenoic acid, 4-[(1H-indol-2-ylmethyl)(phenylmethyl)amino]-3-methyl-, ethyl ester, (2E)-(879375-42-5)
• EPA Substance Registry System: 2-Butenoic acid, 4-[(1H-indol-2-ylmethyl)(phenylmethyl)amino]-3-methyl-, ethyl ester, (2E)-(879375-42-5)

Safety Data

• Hazardous Substances Data: 879375-42-5(Hazardous Substances Data)

Upstream product

• 842127-06-4 (E)-4-bromo-3-methyl-2-butenoyl chloride 
• 100-46-9 benzylamine 
• 19041-16-8 (E)-4-bromo-3-methyl-2-butenoic acid 
• 19005-93-7 1H-indol-2-ylcarboxaldehyde 
• 51318-62-8 ethyl (E)-4-bromo-3-methyl-2-butenoate 
• 149685-64-3 N-((1H-indol-2-yl)methyl)-1-phenylmethanamine 

Downstream Products

• 879375-59-4 carbonic acid 4-[benzyl-(1H-indol-2-ylmethyl)-amino]-3-methyl-but-2-enyl ester methyl ester 
• 879375-50-5 4-[benzyl-(1H-indol-2-ylmethyl)-amino]-3-methyl-but-2-en-1-ol 

Relevant articles and documents

Highly enantioselective synthesis of tetrahydro-β-carbolines and tetrahydro-γ-carbolines via Pd-catalyzed intramolecular allylic alkylation

A novel Pd-catalyzed intramolecular allylic alkylation of indoles allows THBCs and THGCs to be effectively synthesized in high yields and excellent enantiomeric excesses (ee up to 97%). Copyright