941293-02-3

Basic information

• Product Name: (S)-β-4-tert-butoxyphenyl-γ-(S)-N-benzyl-α-methylbenzylamino-propylalcohol
• Synonyms: (S)-β-4-tert-butoxyphenyl-γ-(S)-N-benzyl-α-methylbenzylamino-propylalcohol
• CAS NO: 941293-02-3
• Molecular Weight: 431.618
• Mol File: 941293-02-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-β-4-tert-butoxyphenyl-γ-(S)-N-benzyl-α-methylbenzylamino-propylalcohol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-β-4-tert-butoxyphenyl-γ-(S)-N-benzyl-α-methylbenzylamino-propylalcohol(941293-02-3)
• EPA Substance Registry System: (S)-β-4-tert-butoxyphenyl-γ-(S)-N-benzyl-α-methylbenzylamino-propylalcohol(941293-02-3)

Safety Data

• Hazardous Substances Data: 941293-02-3(Hazardous Substances Data)

Upstream product

• 17480-69-2 (S)-N-benzyl-1-phenylethylamine 
• 941293-00-1 3-(4-tert-butoxyphenyl)propionaldehyde 
• 132307-87-0 3-(4-tert-butoxyphenyl)-propan-1-ol 
• 896721-70-3 (S)-N-benzyl-N-(methoxymethyl)-1-phenylethan-1-amine 
• 15359-98-5 4-(tert-butoxy)toluene 
• 106-44-5 p-cresol 

Downstream Products

• 941293-01-2 C₁₄H₂₃NO₂ 
• 941293-03-4 (s)-β-4-tert-butoxylphenyl-γ-Fmoc-amino-propylalcohol 

Relevant articles and documents

Practical synthesis of enantiomerically pure β2-amino acids via proline-catalyzed diastereoselective aminomethylation of aldehydes

Proline-catalyzed diastereoselective aminomethylation of aldehydes using a chiral iminium ion, generated from a readily prepared precursor, provides α-substituted-β-amino aldehydes with 85:15 to 90: 10 dr. The α-substituted-β-amino aldehydes can be reduce