91373-74-9

Basic information

• Product Name: Benzenepropanol, b-[[(4-methoxyphenyl)methyl]amino]-, (S)-
• CAS NO: 91373-74-9
• Molecular Formula: C17H21NO2
• Molecular Weight: 271.359
• Mol File: 91373-74-9.mol

Chemical Properties

• CAS DataBase Reference: Benzenepropanol, b-[[(4-methoxyphenyl)methyl]amino]-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanol, b-[[(4-methoxyphenyl)methyl]amino]-, (S)-(91373-74-9)
• EPA Substance Registry System: Benzenepropanol, b-[[(4-methoxyphenyl)methyl]amino]-, (S)-(91373-74-9)

Safety Data

• Hazardous Substances Data: 91373-74-9(Hazardous Substances Data)

Upstream product

• 63-91-2 L-phenylalanine 
• 3182-95-4 L-Phenylalaninol 
• 100-07-2 4-methoxy-benzoyl chloride 
• 17817-56-0 (S)-2-{[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-amino}-3-phenyl-propan-1-ol 
• 59490-36-7 (2S)-methyl 2--3-phenyl-1-propanoate 

Downstream Products

• 132207-13-7 (4S)-4-benzyl-3-(p-methoxybenzyl)-1,2,3-oxothiazolidine S-oxide 
• 852468-44-1 ethyl (4S,2E)-4-(4-methoxybenzylamino)-2-methyl-5-phenylpent-2-enoate 
• 852468-43-0 ethyl (4S,2Z)-4-[tert-butoxycarbonyl-(4-methoxybenzyl)amino]-2-methyl-5-phenylpent-2-enoate 
• 852468-42-9 ethyl (4S,2E)-4-[tert-butoxycarbonyl-(4-methoxybenzyl)amino]-2-methyl-5-phenylpent-2-enoate 
• 852468-46-3 ethyl (2R)-2-[(3S,4S)-3-benzyl-2-(4-methoxybenzyl)-1-oxo-2-azaspiro[4.5]decan-4-yl]propanoate 
• 169905-23-1 (S)-2-[N-tert-butoxycarbonyl-N-(4′-Methoxybenzyl)amino]-3-phenylpropionaldehyde 
• 132207-11-5 (2S)-1-azido-2--3-phenyl-propane 
• 132233-11-5 (4S)-4-benzyl-3-(p-methoxybenzyl)-1,2,3-oxothiazolidine S,S-dioxide 
• 132207-12-6 (3S)-3--4-phenylbutyronitrile 
• 132207-10-4 (2S)-1-fluoro-2--3-phenyl-propane 
• 169905-26-4 (S,S)-2-<2--1-hydroxy-3-phenylpropyl>-1,3-thiazole 
• 169905-33-3 (1'S,2'S)-2-<2'--1'-<(tert-butyldimethylsilyl)oxy>-3'-phenylpropyl>-1,3-thiazole 
• 144944-04-7 (2S,3S)-3--2-<(tert-butyldimethylsilyl)oxy>-4-phenylbutanal 
• 169905-25-3 (S,S)-2--3-phenyl-1-(1,3-thiazol-2-yl)propyl acetate 

Relevant articles and documents

Intramolecular Diels-Alder Cycloaddition Approach toward the cis-Fused Δ5,6-Hexahydroisoindol-1-one Core of Cytochalasins

Synthesis of the cis-fused Δ5,6-hexahydroisoindol-1-one core of cytochalasins B2-B5, K, Z8, Z9, Z12-Z15, and Z17 has been established starting from an intramolecular D

Dynamic kinetic resolution during iron carbonyl promoted [6+2] ene-type reactions

Intramolecular coupling of cyclohexadiene-Fe(CO)3 complexes with pendant alkenes, to form spirolactams, proceed with excellent stereocontrol, using chiral amide substrates that lead to dynamic kinetic resolution.

Optically active N-substituted phenylalaninols and use thereof

Optically active N-substituted phenylalaninols of the formula (I): STR1 wherein R is isopropyl, 1-ethylpropyl, cyclopentyl, cyclohexyl, cycloheptyl, 4-methylbenzyl, 4-methoxybenzyl, or 3,4-methylenedioxybenzyl; and acid addition salts thereof which are useful as a resolving agent, and a process for preparing D-3-acetylthio-2-methylpropionic acid which comprises reacting DL-3-acetylthio-2-methylpropionic acid with an optically active N-substituted phenylalaninol of the formula (I) to form diastereomeric salts, subjecting the formed diastereomeric salts to a fractional crystallization from a solvent to separate the D-acid salt from the L-acid salt, and then decomposing the D-acid salt with a mineral acid to give D-3-acetylthio-2-methylpropionic acid.