1618136-61-0

Basic information

• Product Name: C₂₈H₃₃N₃O₆S
• Synonyms: C₂₈H₃₃N₃O₆S
• CAS NO: 1618136-61-0
• Molecular Weight: 539.653
• Mol File: 1618136-61-0.mol

Chemical Properties

• CAS DataBase Reference: C₂₈H₃₃N₃O₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₃₃N₃O₆S(1618136-61-0)
• EPA Substance Registry System: C₂₈H₃₃N₃O₆S(1618136-61-0)

Safety Data

• Hazardous Substances Data: 1618136-61-0(Hazardous Substances Data)

Upstream product

• 85231-15-8 4-formyl-2,5-dimethylphenol 
• 42308-20-3 2-bromopropionanilide 
• 18073-18-2 1,4,9-trimethyl-9H-carbazole-3-carbaldehyde 
• 645-36-3 2,2-diethoxy-ethanamine 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 
• 95-87-4 2,5-Dimethylphenol 
• 1326776-30-0 3-(2,2-diethoxyethylaminomethyl)-1,4,9-trimethylcarbazole 
• 18073-26-2 3-(2,2-diethoxyethyliminomethyl)-1,4,9-trimethylcarbazole 
• 14501-66-7 1,4-dimethylcarbazole-3-carboxaldehyde 

Downstream Products

• 18073-33-1 6-methylellipticine 
• 56501-52-1 6-methyl-9-hydroxyellipticine 
• 1618136-72-3 2-(N-Boc-2-aminoethoxy)ethyl-9-hydroxy-6-methylellipticinium chloride 
• 1618136-76-7 2-(2-aminoethoxy)ethyl-9-hydroxy-6-methylellipticinium chloride 
• 1618136-81-4 C₂₄H₂₉N₄O₃⁽¹⁺⁾*Cl^(1-) 
• 1618136-86-9 C₂₄H₂₈N₅O₄⁽¹⁺⁾*Cl^(1-) 
• 1618136-73-4 2-(N-Boc-5-aminopentyl)-9-hydroxy-6-methylellipticinium chloride 
• 1618136-77-8 2-(5-aminopentyl)-9-hydroxy-6-methylellipticinium chloride 
• 1618136-82-5 Cl^(1-)*C₂₅H₃₁N₄O₂⁽¹⁺⁾ 
• 1618136-87-0 C₂₅H₃₀N₅O₃⁽¹⁺⁾*Cl^(1-) 
• 1618136-67-6 C₂₇H₃₄N₃O₄⁽¹⁺⁾*C₇H₇O₃S^(1-) 
• 1618136-69-8 C₂₈H₃₆N₃O₃⁽¹⁺⁾*C₇H₇O₃S^(1-) 

Relevant articles and documents

A transition metal-free approach to a regioselective total synthesis of the natural product derivative 6-methylellipticine, a potent anticancer agent

A transition metal-free and regioselective total synthesis of 6-methylellipticine, a potent anticancer agent, was developed. This synthetic approach mainly involved two key reactions: a direct amination of multi-functional phenol via an alkylation-Smiles

Synthesis and in vitro antitumor activity of novel 2-alkyl-5- methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazol-2-ium and 2-alkylellipticin-2-ium chloride derivatives

Twenty-one types of novel ellipticine derivatives and pyridocarbazoles (5-methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazoles) with a nitrosourea moiety, linked by an oxydiethylene unit at the 2 position, were synthesized, and their cytotoxicity against HeLa S-3 cells was evaluated. Some of these new compounds exhibited potent antitumor activity by comparison with that of ellipticine.