75849-10-4

Basic information

• Product Name: ethyl 3-<3-(benzyloxy)phenyl>propanoate
• Synonyms: ethyl 3-<3-(benzyloxy)phenyl>propanoate
• CAS NO: 75849-10-4
• Molecular Weight: 284.355
• Mol File: 75849-10-4.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: ethyl 3-<3-(benzyloxy)phenyl>propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-<3-(benzyloxy)phenyl>propanoate(75849-10-4)
• EPA Substance Registry System: ethyl 3-<3-(benzyloxy)phenyl>propanoate(75849-10-4)

Safety Data

• Hazardous Substances Data: 75849-10-4(Hazardous Substances Data)

Upstream product

• 208836-69-5 3-(3'-benzyloxyphenyl)-(E)-propenoic acid ethyl ester 
• 3943-96-2 3-(3-hydroxyphenyl)acrylic acid ethyl ester 
• 96251-92-2 (E)-3-(3-hydroxyphenyl)acrylic acid ethyl ester 
• 14755-02-3 3-hydroxy-trans-cinnamic acid 
• 34708-60-6 3-(3-hydroxy-phenyl)propionic acid ethyl ester 
• 100-39-0 benzyl bromide 
• 621-54-5 3-(3-hydroxyphenyl)-propanoic acid 
• 14755-02-3 3-hydroxycinnamic acid 

Downstream Products

• 121484-77-3 5-(2-(3-(3-benzyloxyphenyl)propamido)phenyl)-10,15,20-triphenylporphyrin 
• 121484-78-4 5-(2-(3-(3-hydroxyphenyl)propamido)phenyl)-10,15,20-triphenylporphyrin 
• 121484-76-2 3-(3-benzyloxy-phenyl)-propionyl chloride 
• 73087-65-7 1-(4-methoxyphenyl)-4-(3-methoxyphenyl)butan-1-ol 
• 75849-12-6 1-(2-benzyloxyphenyl)-4-(3-benzyloxyphenyl)butan-1-ol 
• 75849-22-8 1-(4-benzyloxyphenyl)-4-(3-benzyloxyphenyl)butan-1-ol 
• 73087-66-8 8-methoxy-1-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene 
• 75849-13-7 1-(2-methoxyphenyl)-4-(3-methoxyphenyl)butan-1-ol 
• 75849-11-5 1-(benzyloxy)-3-(3-bromopropyl)benzene 
• 73087-57-7 8-(2-Hydroxy-phenyl)-5,6,7,8-tetrahydro-naphthalen-1-ol 
• 73087-58-8 5-(2-Hydroxy-phenyl)-5,6,7,8-tetrahydro-naphthalen-2-ol 
• 73087-63-5 8-(4-Hydroxy-phenyl)-5,6,7,8-tetrahydro-naphthalen-1-ol 
• 100-39-0 benzyl bromide 
• 73087-64-6 1-(3-Hydroxyphenyl)-5-hydroxytetralin 

Relevant articles and documents

MEDICINAL COMPOSITIONS IMPROVED IN SOLUBLITY IN WATER

Solid dispersions are provided comprising an HER2 inhibitor which is hardly or not soluble in water and a hydrophilic polymer. These solid dispersions have been improved in the solubility of the HER2 inhibitor, oral absorption and bioavailability in blood

Improved synthesis of 5-benzyl-2-thiouracils

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Regioselective synthesis of 1,8-dihydroxytetralins through a tandem reduction/intramolecular hydroxyalkylation of 4-(3-hydroxyphenyl)alkanoates

A series of 4-(3-hydroxyphenyl)butanoates 3 has been prepared and transformed into 1,8-dihydroxytetralins of general formula 2 by treatment with 2 equivalents of DIBALH followed by quenching with aqueous NH4Cl. A possible mechanism for this novel totally regioselective intramolecular hydroxyalkylation is suggested and the factors affecting the stability of 1,8-dihydroxytetralins 2 are also discussed.