64715-81-7

Basic information

• Product Name: (+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE
• Synonyms: (s)-(+)-α-(methoxymethyl)phenethylamine hydrochloride;(+)-O-Methyl-L-phenylalaninol hydrochloride, (S)-(+)-2-Amino-1-methoxy-3-phenylpropane hydrochloride;(+)-O-Methyl-L-phenylalaninol hydrochloride, (S)-(+)-1-Methoxy-3-phenyl-2-propylamine hydrochloride, (S)-(+)-2-Amino-1-methoxy-3-phenylpropane hydrochloride;(S)-1-Methoxy-3-phenylpropan-2-aMine hydrochloride;(S)-(+)-alpha-(Methoxymethyl)phenethylamine hydrochloride 98%;(+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE;(S)-(+)-ALPHA-(METHOXYMETHYL)PHENETHYLAMINE HYDROCHLORIDE;S(+)-2-AMINO-1-METHOXY-3-PHENYLPROPANE HYDROCHLORIDE
• CAS NO: 64715-81-7
• Molecular Formula: C₁₀H₁₅NO*ClH
• Molecular Weight: 201.69
• Mol File: 64715-81-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 149-151 °C
• Boiling Point: 265.4°C at 760 mmHg
• Flash Point: 97.6°C
• Appearance: /
• Density: 0.997g/cm³
• Vapor Pressure: 0.00918mmHg at 25°C
• Refractive Index: 1.519
• Storage Temp.: Inert atmosphere,Room Temperature
• BRN: 5139125
• CAS DataBase Reference: (+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE(64715-81-7)
• EPA Substance Registry System: (+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE(64715-81-7)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 3-10
• Hazardous Substances Data: 64715-81-7(Hazardous Substances Data)

Usage

General Description

(+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE is a chemical compound that is commonly used in the production of pharmaceuticals and other organic chemicals. It is a chiral compound, meaning it has a non-superimposable mirror image, and is often used in the synthesis of other chiral molecules. (+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE is also used as a key intermediate in the synthesis of various pharmaceutical drugs and as a reagent in organic synthesis. It is a white to off-white crystalline powder that is soluble in water and has a variety of potential applications in the pharmaceutical and chemical industries.

InChI:InChI=1/C10H15NO/c1-12-8-10(11)7-9-5-3-2-4-6-9/h2-6,10H,7-8,11H2,1H3/t10-/m0/s1

Upstream product

• 1313186-51-4 (S)-N-(1-benzyl-2-methoxyethyl)-2,4-dinitrophenylsulfonamide 
• 1313186-38-7 (S)-N-(1-benzyl-2-hydroxyethyl)-2,4-dinitrophenylsulfonamide 
• 1313186-43-4 (S)-2-benzyl-1-(2,4-dinitrophenylsulfonyl)aziridine 
• 3182-95-4 L-Phenylalaninol 
• 64715-80-6 (S)-1-benzyl-2-methoxyethylamine 
• 3618-96-0 (S)-N-acetylphenylalanine 
• 52485-51-5 N-[(1S)-1-benzyl-2-hydroxyethyl]acetamide 
• 88382-99-4 C₁₂H₁₇NO₂ 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 21156-62-7 (R)-N-acetylphenylalanine methyl ester 
• 59919-06-1 (R)-N-(1-Benzyl-2-methoxy-aethyl)-acetamid 
• 13033-84-6 D-phenylalanine methyl ester hydrochloride 
• 1009094-66-9 tert-butyl N-[(1R)-1-benzyl-2-methoxyethyl]carbamate 

Downstream Products

• 129156-86-1 (S)-2-isopropylamino-1-methoxy-3-phenylpropane 
• 344799-63-9 (S)-N-(1-benzyl-2-methoxyethyl)-2-hydroxynaphthalenecarboxamide 
• 344799-64-0 (S)-N-(1-benzyl-2-methoxyethyl)-2-(trifluoromethanesulfonyloxy)naphthalenecarboxamide 
• 64715-80-6 (S)-1-benzyl-2-methoxyethylamine 
• 1616107-99-3 C₂₄H₃₀N₂O₃ 
• 1616108-01-0 C₂₅H₃₂N₂O₃ 
• 1616108-03-2 C₂₉H₃₂N₂O₃ 
• 1616108-11-2 C₃₃H₃₄N₂O₃ 
• 1616108-00-9 C₂₄H₃₀N₂O₃ 
• 1616108-02-1 C₂₅H₃₂N₂O₃ 
• 1616108-04-3 C₂₉H₃₂N₂O₃ 
• 1616108-12-3 C₃₃H₃₄N₂O₃ 

Relevant articles and documents

PHENETHYL SUBSTITUTED IMIDAZO[4,5-C]QUINOLINE COMPOUNDS WITH AN N-1 BRANCHED GROUP

Imidazo[4,5-c]quinoline compounds having a substituent that is attached at the N-1 position by a branched group, single enantiomers of the compounds, pharmaceutical compositions containing the compounds, and methods of making the compounds are disclosed.

The dinosyl group: A powerful activator for the regioselective alcoholysis of aziridines

The N-2,4-dinitrophenylsulfonyl group (dinosyl, DNs) was found to be an excellent choice for the N-activation of aziridines towards ring cleavage with primary, secondary, andsterically demanding tertiary alcohols. Alcoholysis does not need any additional