38499-45-5

Basic information

• Product Name: 3-amino-3-(4-methoxyphenyl)propanoic acid hydrochloride
• Synonyms: 3-amino-3-(4-methoxyphenyl)propanoic acid hydrochloride
• CAS NO: 38499-45-5
• Molecular Weight: 231.679
• Mol File: 38499-45-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-amino-3-(4-methoxyphenyl)propanoic acid hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-3-(4-methoxyphenyl)propanoic acid hydrochloride(38499-45-5)
• EPA Substance Registry System: 3-amino-3-(4-methoxyphenyl)propanoic acid hydrochloride(38499-45-5)

Safety Data

• Hazardous Substances Data: 38499-45-5(Hazardous Substances Data)

Upstream product

• 1272676-13-7 C₁₈H₂₉NO₄S 
• 131791-77-0 (S)-2-tert-Butyl-6-(4-methoxy-phenyl)-5,6-dihydro-3H-pyrimidin-4-one 
• 864871-39-6 diethyl 2-(1-(N-tert-butoxycarbonylamino)-1-(4-methoxyphenyl)methyl)malonate 
• 365441-82-3 N-(tert-butoxycarbonyl)-α-(4-methylphenylsulfonyl)-4-methoxybenzylamine 

Downstream Products

• 167887-35-6 3-amino-3-(4-methoxyphenyl)propionic acid ethyl ester hydrochloride 
• 57083-19-9 (S)-3-Formylamino-3-(4-methoxy-phenyl)-propionic acid 

Relevant articles and documents

SmI2-promoted imino-Reformatsky reaction for facile synthesis of enantioenriched β-amino acid esters

A facile and efficient method for the stereoselective synthesis of β-amino acid esters via SmI2-promoted imino-Reformatsky reaction is described. Asymmetric addition of tert-butyl bromoacetate to N-tert-butanesulfinyl aldimines afforded β-amino

Self-Reproduction of Chirality. Asymmetric Synthesis of β-Aryl-β-amino Acids from Enantiomerically Pure Dihydropyrimidinones

Enantiomerically pure dihydropyrimidinone 1 reacts with aryl iodides in the presence of catalytic amounts of Pd(OAc)2 and added phosphine to afford dihydropyrimidinone 4, in which a formal conjugate addition of the aryl group to the α,β-unsaturated system