4219-94-7

Basic information

• Product Name: O-methylserine
• Synonyms: O-methylserine;Serine, o-methyl-;O-Methyl-D-serine;DL-Serine, O-Methyl-
• CAS NO: 4219-94-7
• Molecular Formula: C₄H₉NO₃
• Molecular Weight: 119.1192
• Mol File: 4219-94-7.mol
• Article Data: 8

Chemical Properties

• Melting Point: 210-215℃
• Boiling Point: 260.6°Cat760mmHg
• Flash Point: 111.4°C
• Appearance: /
• Density: 1.195g/cm³
• Vapor Pressure: 0.00363mmHg at 25°C
• Refractive Index: 1.462
• Water Solubility: soluble
• CAS DataBase Reference: O-methylserine(CAS DataBase Reference)
• NIST Chemistry Reference: O-methylserine(4219-94-7)
• EPA Substance Registry System: O-methylserine(4219-94-7)

Safety Data

• Safety Statements: S24/25:
• Hazardous Substances Data: 4219-94-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C4H9NO3/c1-8-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)

Upstream product

• 98632-99-6 O-Methyl-N-acetyl-DL-serine 
• 51293-45-9 O-methyl-N,N-phthaloyl-L-serine 
• 98026-05-2 α-amino-β-methoxy-propionamide 
• 1356449-88-1 calyxamide B 
• 1356449-87-0 calyxamide A 
• 1190855-79-8 neomastoidin A 
• 124-41-4 sodium methylate 

Downstream Products

• 86118-11-8 D-o-methylserine 
• 159610-93-2 Fmoc-O-methyl-L-serine 
• 148278-96-0 (R)-2-amino-3-methoxy-propan-1-ol 
• 327051-11-6 O-methyl-L-serine methyl ester hydrochloride 
• 51293-47-1 N-tert-butoxycarbonyl-(S)-O-methyl-serin 
• 86096-33-5 N-Chloroacetyl-dl-O-methylserine 
• 56-45-1 L-serin 
• 121470-74-4 N-benzoyl-DL-O-methylserine 

Relevant articles and documents

Marine Cyanobacterial Fatty Acid Amides Acting on Cannabinoid Receptors

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PROCESS FOR PREPARING LACOSAMIDE

The present invention provides a process for the preparation of lacosamide in substantially optically pure form, which in one aspect comprises the following steps: (i) resolution of O-methyl-D,L-serine to provide O-methyl-D-serine in substantially optically pure form; (ii) acetylation of O-methyl-D-serine thereby obtained to provide the N-acetyl 10 derivative thereof in substantially optically pure form; (iii) activating the carboxy group of the compound thereby obtained; and (iv) reacting the compound thereby obtained with benzylamine.

Neomastoidin A, a novel monoacylglycerol with an amino acid moiety from Macrolepiota neomastoidea

A novel monoacylglycerol with an amino acid moiety, neomastoidin A (1), was isolated from the fruiting bodies of the poisonous mushroom Macrolepiota neomastoidea. The structure of 1 was established by extensive spectroscopic analysis and further confirmed