133946-40-4

Basic information

• Product Name: <1-3H>-3-phenylpropanal
• Synonyms: <1-3H>-3-phenylpropanal
• CAS NO: 133946-40-4
• Molecular Weight: 136.17
• Mol File: 133946-40-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: <1-3H>-3-phenylpropanal(CAS DataBase Reference)
• NIST Chemistry Reference: <1-3H>-3-phenylpropanal(133946-40-4)
• EPA Substance Registry System: <1-3H>-3-phenylpropanal(133946-40-4)

Safety Data

• Hazardous Substances Data: 133946-40-4(Hazardous Substances Data)

Upstream product

• 131946-57-1 1-phenyl-2-(4,4,6-trimethyl-5,6-dihydro-4H-[1,3]oxazin-2-yl)-ethanol 
• 1462-75-5 3-phenylpropylmagnesium bromide 
• 40228-02-2 5,6-dihydro-2-(2-phenylethyl)-4,4,6-trimethyl-1,3-oxazine 
• 178626-04-5 3-phenyl-1-(2′,2′,6′,6′-tetramethyl-1′-piperidinyloxy)-propane 
• 133946-39-1 <1-3H>-3-phenylprop-2-enal 

Downstream Products

• 64-86-8 colchicine 

Relevant articles and documents

MECHANISM OF THE OXIDATION OF ALCOHOLS BY 2,2,6,6-TETRAMETHYLPIPERIDINE NITROSONIUM CATION

Simple Hammett studies, hydrogen isotope effects, and attempted preparation of proposed transient intermediates are used to probe the mechanism of oxidation of alcohols by 2,2,6,6-tetramethylpiperidine nitrosonium ion.

THE BIOSYNTHESIS OF THE PHENETHYLISOQUINOLINE ALKALOID, COLCHICINE, FROM CINNAMALDEHYDE AND DIHYDROCINNAMALDEHYDE

The important phenethylisoquinoline alkaloid, colchicine (10) is shown to derive from cinnamic acid (5) via cinnamaldehyde (6) and dihydrocinnamaldehyde (7); dihydrocinnamic acid (4) may be used by a minor pathway.