99522-58-4

Basic information

• Product Name: (E)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)prop-2-en-1-ol
• Synonyms: (E)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)prop-2-en-1-ol
• CAS NO: 99522-58-4
• Molecular Weight: 234.295
• Mol File: 99522-58-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)prop-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)prop-2-en-1-ol(99522-58-4)
• EPA Substance Registry System: (E)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)prop-2-en-1-ol(99522-58-4)

Safety Data

• Hazardous Substances Data: 99522-58-4(Hazardous Substances Data)

Upstream product

• 1166391-14-5 (E)-methyl 3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl) acrylate 

Downstream Products

• 103909-81-5 (E)-3-(4-(tetrahydro-2H-pyran-2yloxy)phenyl)acryl aldehyde 

Relevant articles and documents

Synthesis of two alnustone-like natural diarylheptanoids via 4+3 strategy

The first total synthesis of (4E,6E)-1,7-bis(3,4-dihydroxyphenyl)-hepta-4, 6-dien-3-one and an alternative synthesis of (4E,6E)-1,7-bis(4-hydroxyphenyl)- hepta-4,6-dien-3-one, two natural diarylheptanoids, mainly based on Claisen-Schmidt condensation were described. The crucial steps of the syntheses were the condensation of OH-protected 4-aryl-2-butanones with OH-protected 3-aryl-acrylaldehydes by the in situ enamination and then deprotection of OH groups to give the corresponding natural diarylheptanoids. Copyright Taylor & Francis Group, LLC.