207402-09-3

Basic information

• Product Name: 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-5-formyl-2,4-dimethoxy-benzoic acid methyl ester
• Synonyms: 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-5-formyl-2,4-dimethoxy-benzoic acid methyl ester
• CAS NO: 207402-09-3
• Molecular Weight: 474.595
• Mol File: 207402-09-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-5-formyl-2,4-dimethoxy-benzoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-5-formyl-2,4-dimethoxy-benzoic acid methyl ester(207402-09-3)
• EPA Substance Registry System: 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-5-formyl-2,4-dimethoxy-benzoic acid methyl ester(207402-09-3)

Safety Data

• Hazardous Substances Data: 207402-09-3(Hazardous Substances Data)

Upstream product

• 77-78-1 dimethyl sulfate 
• 207398-35-4 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-5-formyl-2,4-dihydroxy-benzoic acid methyl ester 
• 74-88-4 methyl iodide 
• 192385-50-5 4-pivaloyloxy-2-butynal 

Downstream Products

• 207398-36-5 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-2,4-dimethoxy-5-methyl-benzoic acid methyl ester 
• 60435-90-7 5,7-dimethoxy-6-(5-methoxycarbonyl-3-methyl-2-pentenyl)-4-methylphthalide 
• 38877-93-9 7-O-Methylmycophenolic acid 
• 24280-93-1 mycophenolic acid 
• 31858-66-9 methyl mycophenolate 
• 207402-10-6 3-((E)-3,7-Dimethyl-octa-2,6-dienyl)-6-(2,2-dimethyl-propionyloxymethyl)-5-hydroxymethyl-2,4-dimethoxy-benzoic acid methyl ester 

Relevant articles and documents

Total synthesis of mycophenolic acid

A convergent total synthesis of the natural compound mycophenolic acid 1 is described. The synthetic strategy for the construction of the hexasubstituted aromatic nucleus was based on a ring annulation sequence, involving a Michael addition reaction and intramolecular Dieckmann condensation reaction in situ as the key step. Subsequent transformations of the substituents afforded the target mycophenolic acid 1.