1333378-12-3

Basic information

• Product Name: C₃₁H₃₁N₇O₄S₂
• Synonyms: C₃₁H₃₁N₇O₄S₂
• CAS NO: 1333378-12-3
• Molecular Weight: 629.764
• Mol File: 1333378-12-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₁H₃₁N₇O₄S₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₁H₃₁N₇O₄S₂(1333378-12-3)
• EPA Substance Registry System: C₃₁H₃₁N₇O₄S₂(1333378-12-3)

Safety Data

• Hazardous Substances Data: 1333378-12-3(Hazardous Substances Data)

Upstream product

• 1094172-65-2 C₂₀H₂₁BrN₂O₄ 
• 1094172-74-3 C₂₇H₂₇BrN₂O₆S 
• 1094172-75-4 C₂₀H₂₁BrN₂O₅S 
• 1094172-66-3 C₂₅H₂₉BrN₂O₇S 
• 1094172-67-4 C₃₆H₅₀N₂O₇SSi 
• 1094172-76-5 C₂₇H₃₀N₂O₇S 
• 1094172-61-8 C₂₇H₃₁BrN₂O₇S 
• 1094172-71-0 C₃₈H₄₂N₄O₈S₂ 
• 1094172-72-1 C₃₆H₄₀N₄O₇S₂ 
• 1094172-73-2 C₄₃H₄₆N₄O₉S₃ 
• 1094172-58-3 C₁₁H₁₃BN₂O₃S 
• 1333378-30-5 C₃₆H₃₉N₇O₆S₂ 
• 85598-13-6 1-bromo-4-methoxy-2-methyl-3-nitro-benzene 
• 20075-26-7 1-(methoxymethyl)imidazole 

Downstream Products

• 1333378-11-2 C₄₁H₃₅BrN₈O₆S₂ 

Relevant articles and documents

Synthetic studies on dragmacidin D: Synthesis and assembly of three fragments towards an advanced intermediate

We report herein the approach to the key advanced intermediate in the synthesis of the bioactive marine natural product dragmacidin D. By employing a modular synthesis strategy of three fragments (5, 7, and 8), the advanced intermediate 3 has been successfully synthesized in 2.5% yield over 15 steps by starting from nitrotoluene 20. The synthesis also involves sequential cross-coupling reactions, namely Sonogashira and Suzuki-Miyaura reactions, so that various analogues can be efficiently synthesized, which will allow the study of structure-activity relationships of dragmacidin D.