1094172-70-9

Basic information

• Product Name: C₃₅H₃₅N₃O₈S₂
• Synonyms: C₃₅H₃₅N₃O₈S₂
• CAS NO: 1094172-70-9
• Molecular Weight: 689.81
• Mol File: 1094172-70-9.mol

Chemical Properties

• CAS DataBase Reference: C₃₅H₃₅N₃O₈S₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₅H₃₅N₃O₈S₂(1094172-70-9)
• EPA Substance Registry System: C₃₅H₃₅N₃O₈S₂(1094172-70-9)

Safety Data

• Hazardous Substances Data: 1094172-70-9(Hazardous Substances Data)

Upstream product

• 1094172-58-3 C₁₁H₁₃BN₂O₃S 
• 1094172-69-6 C₂₄H₂₄BrNO₇S 
• 67319-05-5 1-(methoxymethyl)-2-(phenylthio)-1H-imidazole 
• 98-59-9 p-toluenesulfonyl chloride 
• 20075-26-7 1-(methoxymethyl)imidazole 
• 1333378-28-1 C₂₄H₂₃NO₇S 
• 1333378-27-0 C₂₃H₂₃NO₅S 
• 1333378-26-9 C₃₂H₄₃NO₅SSi 
• 1333378-25-8 C₂₁H₂₂BrNO₅S 
• 1333378-24-7 C₁₈H₁₈BrNO₅S 
• 1333378-23-6 C₁₉H₁₆BrNO₆S 
• 1333378-22-5 C₁₂H₁₀BrNO₄ 

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.

Synthetic studies on dragmacidin D: synthesis of the left-hand fragment

We report a synthesis of a left-hand fragment of bis(indole)-class marine alkaloid, dragmacidin D. The synthesis features Suzuki-Miyaura reaction for the coupling of imidazolyl boronic acid and (4-indolyl)vinyl bromide.