51985-42-3

Basic information

• Product Name: methyl 5-methoxy-2-(methoxymethyloxy)benzoate
• Synonyms: methyl 5-methoxy-2-(methoxymethyloxy)benzoate
• CAS NO: 51985-42-3
• Molecular Weight: 226.229
• Mol File: 51985-42-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 5-methoxy-2-(methoxymethyloxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-methoxy-2-(methoxymethyloxy)benzoate(51985-42-3)
• EPA Substance Registry System: methyl 5-methoxy-2-(methoxymethyloxy)benzoate(51985-42-3)

Safety Data

• Hazardous Substances Data: 51985-42-3(Hazardous Substances Data)

Upstream product

• 94420-55-0 methyl 2-hydroxy-5-(tetrahydropyranyloxy)benzoate 
• 179749-30-5 2-Methoxymethoxy-5-(tetrahydro-pyran-2-yloxy)-benzoic acid methyl ester 
• 2150-46-1 Methyl 2,5-dihydroxybenzoate 
• 2905-82-0 methyl 5-methoxy-2-hydroxybenzoate 
• 107-30-2 chloromethyl methyl ether 
• 144033-76-1 5-Hydroxy-2-methoxymethoxy-benzoic acid methyl ester 
• 74-88-4 methyl iodide 

Downstream Products

• 179915-23-2 (1S,2R,6R)-1-(5-Methoxy-2-methoxymethoxy-benzyl)-2,6-dimethyl-2-((E)-4-methyl-penta-1,3-dienyl)-cyclohexanol 
• 179749-27-0 2-[(R)-2,6-Dimethyl-6-((E)-4-methyl-penta-1,3-dienyl)-cyclohex-1-enylmethyl]-4-methoxy-1-methoxymethoxy-benzene 
• 179749-15-6 2-Chloromethyl-4-methoxy-1-methoxymethoxy-benzene 
• 422566-54-9 11-benzyloxy-2,12-dimethoxy-14-(4-benzyloxy-3-methoxyphenyl)-6H[1]benzopyrano[4',3':4,5]pyrrolo[2,1-a]isoquinoline-6-one 
• 422566-47-0 6-benzyloxy-7-methoxy-1-[1-(4-benzyloxy-3-methoxyphenyl)-2-(5-methoxy-2-methoxymethoxyphenyl)-2-oxoethyl]isoquinoline 
• 179749-31-6 (5-methoxy-2-(methoxymethoxy)phenyl)-methan-1-ol 

Relevant articles and documents

Synthesis and structure-activity relationship study of lamellarin derivatives

Ten derivatives (3-12) of marine alkaloid lamellarin D (1) were synthesized and evaluated for cytotoxicity against a HeLa cell line in an effort to examine their structure-activity relationships. It appeared that the hydroxyl groups at positions C-8 and C-20 of 1 were important structural requirements for cytotoxic activity, while the hydroxyl group at C-14 and the two methoxy groups at C-13 and C-21 were not necessary for the activity.