1425861-04-6

Basic information

• Product Name: 4-hydroxy-6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-2,3-dihydro-isoindol-1-one
• Synonyms: 4-hydroxy-6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-2,3-dihydro-isoindol-1-one
• CAS NO: 1425861-04-6
• Molecular Weight: 373.406
• Mol File: 1425861-04-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-hydroxy-6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-2,3-dihydro-isoindol-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-2,3-dihydro-isoindol-1-one(1425861-04-6)
• EPA Substance Registry System: 4-hydroxy-6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-2,3-dihydro-isoindol-1-one(1425861-04-6)

Safety Data

• Hazardous Substances Data: 1425861-04-6(Hazardous Substances Data)

Upstream product

• 1425861-07-9 [2-(4-methoxymethoxyphenyl)ethyl]carbamic acid benzyl ester 
• 29655-46-7 N-benzyloxycarbonyl-2-(4-hydroxyphenyl)ethylamine 
• 439600-45-0 2-formyl-3-hydroxy-5-methoxymethoxy-benzoic acid methyl ester 
• 16849-78-8 2-formyl-3,5-dihydroxybenzoic acid methyl ester 

Downstream Products

• 1425861-26-2 (E)-8-(4,8-dimethylnona-3,7-dienyl)-5-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-8-methyl-1,2-dihydro-8H-9-oxa-2-azacyclopenta[a]naphthalen-3-one 
• 1425861-34-2 (E)-8-(4,8-dimethylnona-3,7-dienyl)-5-hydroxy-2-[2-(4-hydroxyphenyl)ethyl]-8-methyl-1,2-dihydro-8H-9-oxa-2-azacyclopenta[a]naphthalen-3-one 
• 1425861-23-9 C₃₅H₄₅NO₆ 
• 1445069-52-2 4-hydroxy-6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-5-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)-2,3-dihydroisoindol-1-one 
• 1445069-56-6 4-hydroxy-6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-5-((2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)-2,3-dihydroisoindol-1-one 
• 1445069-48-6 6-methoxymethoxy-2-[2-(4-methoxymethoxyphenyl)ethyl]-4-((E)-1,5,9-trimethyl-1-vinyldeca-4,8-dienyloxy)-2,3-dihydroisoindol-1-one 

Relevant articles and documents

Synthetic studies towards stachybotrin C

The preparation of racemic des-hydroxy stachybotrin C is described. Different approaches have been studied. Observations made in the course of the synthesis show the efficiency of the intermolecular cyclization between the diethyl acetal 19 and phenol 12 leading to the benzopyran moiety 17. Georg Thieme Verlag KG · Stuttgart · New York.