1403963-34-7

Basic information

• Product Name: C₂₉H₃₈N₂O₃
• Synonyms: C₂₉H₃₈N₂O₃
• CAS NO: 1403963-34-7
• Molecular Weight: 462.632
• Mol File: 1403963-34-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₉H₃₈N₂O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₉H₃₈N₂O₃(1403963-34-7)
• EPA Substance Registry System: C₂₉H₃₈N₂O₃(1403963-34-7)

Safety Data

• Hazardous Substances Data: 1403963-34-7(Hazardous Substances Data)

Upstream product

• 1237706-56-7 1,3-bis-(2,4,6-trimethylphenyl)-4,6-diketo-5,5-dimethylpyrimidin-2-ylidene 
• 555-16-8 4-nitrobenzaldehdye 
• 630-19-3 pivalaldehyde 
• 2043-61-0 cyclohexanecarbaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-52-7 benzaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 124-13-0 Octanal 
• 1237706-56-7 1,3-bis-(2,4,6-trimethylphenyl)-4,6-diketo-5,5-dimethylpyrimidin-2-ylidene 
• 630-19-3 pivalaldehyde 
• 555-16-8 4-nitrobenzaldehdye 
• 1122-91-4 4-bromo-benzaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 100-52-7 benzaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 2043-61-0 cyclohexanecarbaldehyde 

Relevant articles and documents

Elucidating the mechanism of reversible oxiranations via magnetization transfer spectroscopy

The reversible [2 + 1] cycloadditions between an N,N′-diamidocarbene (DAC) and eight aldehydes were examined using NMR spectroscopy. Variable temperature magnetization transfer experiments revealed higher exchange rates and lower activation barriers when electron-deficient aldehydes were employed. Likewise, competitive equilibrium studies indicated a thermodynamic preference for electron-deficient aryl and sterically unhindered alkyl aldehydes compared to more electron-rich or bulkier substrates. Collectively, these and other data collected were consistent with the oxiranation process proceeding in an asynchronous manner.