214271-70-2

Basic information

• Product Name: methyl (Z)-3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate
• Synonyms: methyl (Z)-3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate
• CAS NO: 214271-70-2
• Molecular Weight: 368.386
• Mol File: 214271-70-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl (Z)-3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (Z)-3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate(214271-70-2)
• EPA Substance Registry System: methyl (Z)-3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate(214271-70-2)

Safety Data

• Hazardous Substances Data: 214271-70-2(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 120-57-0 piperonal 
• 150356-60-8 methyl 3-(prop-1-yloxy)benzoylacetate 
• 121704-77-6 3-(prop-1-yloxy)acetophenone 

Relevant articles and documents

An unprecedented asymmetric Nazarov cyclization for the synthesis of nonracemic indanes as endothelin receptor antagonists

An asymmetric synthesis of the novel nonracemic endothelin receptor antagonists, SB 209670 (1a) and SB 217242 (1b) is described which utilizes an unprecedented asymmetric Nazarovtype ring closure of the alkylidene-1,3- carbonyl compounds. Excellent 1,5-induction is observed which establishes the required S configuration at the C-3 carbon of an indane skeleton.

ENDOTHELIN RECEPTOR ANTAGONISTS

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