55104-60-4

Basic information

• Product Name: methyl 3-allyloxy-5-methoxybenzoate
• Synonyms: methyl 3-allyloxy-5-methoxybenzoate
• CAS NO: 55104-60-4
• Molecular Weight: 222.241
• Mol File: 55104-60-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl 3-allyloxy-5-methoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-allyloxy-5-methoxybenzoate(55104-60-4)
• EPA Substance Registry System: methyl 3-allyloxy-5-methoxybenzoate(55104-60-4)

Safety Data

• Hazardous Substances Data: 55104-60-4(Hazardous Substances Data)

Upstream product

• 19520-74-2 3-hydroxy-5-methoxy-benzoic acid methyl ester 
• 106-95-6 allyl bromide 
• 1458-98-6 2-methyl-3-bromo-1-propene 
• 19520-75-3 3-hydroxy-5-methoxybenzoic acid 

Downstream Products

• 55703-71-4 4-allyl-3-hydroxy-5-methoxybenzoic acid 
• 55703-72-5 2-allyl-3-hydroxy-5-methoxybenzoic acid 
• 68787-63-3 methyl 2,3-dihydro-6-methoxy-2-methyl-4-benzofurancarboxylate 
• 55104-61-5 3-allyloxy-5-methoxybenzoic acid 
• 1539304-70-5 C₂₁H₂₅N₅O₇ 
• 1539304-69-2 C₁₁H₁₃ClO₂ 

Relevant articles and documents

Rhodium-Catalyzed Twofold Unsymmetrical C-H Alkenylation-Annulation/Thiolation Reaction to Access Thiobenzofurans

A Rh(III)-catalyzed twofold unsymmetrical C-H alkenylation-annulation/thiolation reaction has been developed, enabling the straightforward and efficient synthesis of various thiobenzofurans in one step. This robust protocol proceeds with a broad substrate scope and good functional group tolerance under relatively mild reaction conditions.

SYNTHESIS OF 4-ALKENYL-3,5-DIMETHOXYBENZOIC ACIDS BY CLAISEN REARRANGEMENT

Methyl 3-allyloxy-5-methoxybenzoate (1a) and its methyl homologues on the α, β and γ carbon atoms (1b,c,d) have been subjected to Claisen rearrangement.The structures of the rearranged products have been determined and the factors affecting the isomeric r

AMINOPROPANOL SUBSTITUTED ISOCHROMANONES AND PHTHALIDES

Aminopropanols with β-blocking activity having the general formula SPC1Wherein R is hydrogen, C 1-C 4 alkyl or hydroxy-(C 2-C 4) alkyl, R 1 is C 1-C 4 alkyl or hydroxy-(C 2-C 4) alkyl; R 2 and R 3 each independently represent hydrogen or C 1-C 2 alk