6522-01-6

Basic information

• Product Name: METHYL 3-(4-(ALLYLOXY)PHENYL)PROPANOATE
• Synonyms: METHYL 3-(4-(ALLYLOXY)PHENYL)PROPANOATE
• CAS NO: 6522-01-6
• Molecular Formula: C₁₃H₁₆O₃
• Molecular Weight: 220.26
• Mol File: 6522-01-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: METHYL 3-(4-(ALLYLOXY)PHENYL)PROPANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3-(4-(ALLYLOXY)PHENYL)PROPANOATE(6522-01-6)
• EPA Substance Registry System: METHYL 3-(4-(ALLYLOXY)PHENYL)PROPANOATE(6522-01-6)

Safety Data

• Hazardous Substances Data: 6522-01-6(Hazardous Substances Data)

Upstream product

• 5597-50-2 3-(4-hydroxyphenyl)propionic acid methyl ester 
• 106-95-6 allyl bromide 
• 7400-08-0 p-Coumaric Acid 

Downstream Products

• 83812-23-1 methyl-3(3-allyl-4-hydroxyphenyl)propionate 
• 6522-02-7 3-(4-(allyloxy)phenyl)propanoic acid 
• 515834-96-5 3-(4-allyloxy-phenyl)-propionic acid but-3-enyl ester 
• 515834-99-8 3-(4-allyloxy-phenyl)-propionic acid pent-4-enyl ester 
• 515835-01-5 3-(4-allyloxy-phenyl)-propionic acid hex-5-enyl ester 
• 166959-39-3 3-(3-Allyl-4-trifluoromethanesulfonyloxy-phenyl)-propionic acid methyl ester 
• 219502-08-6 3-(4-allyloxyphenyl)propanoyl chloride 
• 1610043-25-8 5-(3-(4-(allyloxy)phenyl)propanoyl)-1H-pyrrole-2-carboxylic acid 
• 1610043-27-0 methyl (2S)-2-[[5-[3-(4-allyloxyphenyl)propanoyl]-1H-pyrrole-2-carbonyl]amino]pent-4-enoate 
• 1610043-28-1 methyl (2S)-3-(4-allyloxyphenyl)-2-[[5-[3-(4-allyloxyphenyl)propanoyl]-1H-pyrrole-2-carbonyl]amino]propanoate 
• 1610043-18-9 (S)-N-((S)-1-hydroxy-3-phenylpropan-2-yl)-2,13-dioxo-11H-6-oxa-12-aza-1(2,5)-pyrrola-5(1,4)-benzenacyclotridecaphane-11-carboxamide 

Relevant articles and documents

MACROCYCLIC COMPOUNDS AND USES THEREOF

The present invention relates to novel macrocyclic compounds of Formula I and their use as novel therapeutic agents for example as novel compounds used in methods of preventing and/or treating a disease, condition or state in a subject associated with dysregulation of protease activity and/or dysregulation of proteosome activity

Synthetic approach to pondaplin and highly strained ansa macrolides: The dramatic influence of a fluorine atom on the efficiency of ring-closing metathesis

Ring-closing metathesis has been applied to the synthesis of extremely rigid 13 to 16 membered ring lactones starting from alkenyl p-(O-allyl)cinnamates and p-(O-allyl)dihydrocinnamates. The core structure of pondaplin, a natural ansa macrolide has been prepared starting from a fluoro derivative. The presence of this atom seems to have a crucial role on the success of the RCM.