155627-09-1

Basic information

• Product Name: ethyl <4-(methoxy)methoxy>phenylacetate
• Synonyms: ethyl <4-(methoxy)methoxy>phenylacetate
• CAS NO: 155627-09-1
• Molecular Weight: 224.257
• Mol File: 155627-09-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl <4-(methoxy)methoxy>phenylacetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl <4-(methoxy)methoxy>phenylacetate(155627-09-1)
• EPA Substance Registry System: ethyl <4-(methoxy)methoxy>phenylacetate(155627-09-1)

Safety Data

• Hazardous Substances Data: 155627-09-1(Hazardous Substances Data)

Upstream product

• 17138-28-2 (4-hydroxy-phenyl)-acetic acid ethyl ester 
• 107-30-2 chloromethyl methyl ether 
• 156-38-7 4-hydroxyphenylacetate 

Downstream Products

• 155626-96-3 ethyl 4-(1,3-dioxolan-2-yl)-2-(4-methoxymethoxyphenyl)butyrate 
• 155626-98-5 1-benzyloxy-4-(1,3-dioxolan-2-yl)-2-(4-methoxymethoxyphenyl)butane 
• 155627-00-2 7-Benzyloxy-2-diazo-6-(4-hydroxy-phenyl)-heptan-3-one 
• 94194-08-8 4-(4-acetoxyphenyl)-5-benzyloxypentanoic acid 
• 155627-08-0 5-Benzyloxy-4-(4-hydroxy-phenyl)-pentanal 
• 155626-97-4 4-[1,3]Dioxolan-2-yl-2-(4-methoxymethoxy-phenyl)-butan-1-ol 
• 169888-76-0 2-<4-(methoxy)methoxy>phenyl-1,3-propanediol 
• 169888-82-8 diethyl <4-(methoxy)methoxy>phenylmalonate 

Relevant articles and documents

Vanilloid Receptor Ligands, Pharmaceutical Compositions Containing Them, Process for Making Them, and Use Thereof for Treating Pain and Other Conditions

Vanilloid receptor ligand compounds corresponding to formula I: pharmaceutical compositions containing such compounds, a process for producing such compounds, and methods of using such compounds for treating or inhibiting pain and various other disorders or conditions.

Synthetic studies on aphidicolane and stemodane diterpenes. II. Neighboring hydroxyl group participation in stereoselective syntheses of tricyclo[6.3.1.01,6]dodecanes corresponding to the B/C/D-ring systems

Tricyclo[6.3.1.01,6]dodecane derivatives (5 and 6) corresponding to the B/C/D-ring systems of aphidicolane and stemodane diterpenes were synthesized stereoselectively via a spirodienone-alcohol (4) as a common intermediate. Participation of the neighboring hydroxyl group in 4 is crucial for controlling the stereochemistry of the spirocenters.