55103-94-1

Basic information

• Product Name: C₁₁H₁₄⁽²⁾HN
• CAS NO: 55103-94-1
• Molecular Weight: 162.239
• Mol File: 55103-94-1.mol

Chemical Properties

• CAS DataBase Reference: C₁₁H₁₄⁽²⁾HN(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₁H₁₄⁽²⁾HN(55103-94-1)
• EPA Substance Registry System: C₁₁H₁₄⁽²⁾HN(55103-94-1)

Safety Data

• Hazardous Substances Data: 55103-94-1(Hazardous Substances Data)

Upstream product

• 101960-59-2 [(Z)-Butylimino]-phenyl-acetic acid 
• 98-88-4 benzoyl chloride 
• 21175-64-4 1,1-dideuteriophenylmethanol 
• 3592-47-0 Benzaldehyde-d 
• 109-73-9 N-butylamine 

Relevant articles and documents

Phosphites mediated decarboxylation of α-iminoacids. A straightforward route to labelled α-aminophosphates

Aminophosphates are of great interest owing to their biological activity. These products are considered as structural analogues of the corresponding aminoacids but also as transition state mimics of peptide hydrolysis. They are known to act as antibiotic and pharmacological agents as well as enzyme inhibitors. Despite the growing importance of these drugs, few methods have been reported for their labelling. These isotopic syntheses usually involve strong bases to generate an α-carbanion which is then quenched with D2O. In the present article we would like to report two novel procedures for the one pot synthesis of labelled α-aminophosphates. These procedures could easily be adapted to tritium labelling.

Radical Cations from N-Alkyl Substituted Imines: an EPR Study

Following γ-radiolysis of dilute solutions of imines in trichlorofluoromethane at 77 K, EPR spectra of the corresponding radical cations were recorded.For PhCH=NEt amnd PhCH=NCHMe2 the primary 2A' cations were formed, but in each case as a mixt