2566-32-7

Basic information

• Product Name: N-ME-DL-VAL-OH HCL
• Synonyms: N-METHYL-DL-VALINE HYDROCHLORIDE;N-ME-DL-VAL-OH HCL;N-Methyl-dl-valine, HCl;(S)-3-Methyl-2-(MethylaMino)butanoic acid hydrochloride;N-Methylvaline hydrochloride;(2S)-3-methyl-2-methylaminobutanoic acid hydrochloride;(2S)-3-methyl-2-methylamino-butanoic acid hydrochloride;(2S)-3-methyl-2-methylamino-butyric acid hydrochloride
• CAS NO: 2566-32-7
• Molecular Formula: C₆H₁₃NO₂
• Molecular Weight: 167.63
• Product Categories: Amino Acids;I - Z;Modified Amino Acids
• Mol File: 2566-32-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 82-84℃
• Boiling Point: 206.9±23.0 °C(Predicted)
• Appearance: /
• Density: 0.995
• Storage Temp.: Store at RT.
• PKA: 2.38±0.13(Predicted)
• CAS DataBase Reference: N-ME-DL-VAL-OH HCL(CAS DataBase Reference)
• NIST Chemistry Reference: N-ME-DL-VAL-OH HCL(2566-32-7)
• EPA Substance Registry System: N-ME-DL-VAL-OH HCL(2566-32-7)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 2566-32-7(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Uses

N-Methyl-dl-valine, HCl

Definition

ChEBI: An N-methylamino acid that is the N-methyl derivative of valine.

Upstream product

• 1494680-68-0 ohmyungsamycin A 

Downstream Products

• 53358-08-0 N-Nitroso-N-methyl-valin 
• 42492-62-6 2-(benzyl(methyl)amino)-3-methylbutanoic acid 
• 812788-74-2 (3R,6S)-3,6-diisopropyl-4-methyl-2,5-morpholinedione 
• 1007880-07-0 2-(benzyl(methyl)amino)-3-methylbutanoic acid trifluoroacetic acid salt 
• 53978-73-7 Z-D-MeVal 
• 42417-65-2 Z-MeVal-OH 
• 408507-19-7 3-(N-methylamino)-4-methyl-2-pentanone 
• 150715-06-3 5-isopropyl-1-methyl-3-phenyl-2-thiohydantoin 
• 812788-12-8 (3S,6R)-3,6-diisopropyl-4-methyl-2,5-morpholinedione 
• 96893-60-6 DL-N-(4-Nitro-benzyoxycarbonyl)-N-methyl-valin 
• 4216-94-8 N-(4-Nitro-benzyloxycarbonyl)-N-methyl-L-valin 
• 92619-25-5 N-Me-Cbz-valine 
• 13850-91-4 Boc-(D,L)-N(Me)-Val-OH 
• 859800-36-5 N-methyl-N-DL-phenylacetyl-valine 

Relevant articles and documents

Dudawalamides A-D, Antiparasitic Cyclic Depsipeptides from the Marine Cyanobacterium Moorea producens

A family of 2,2-dimethyl-3-hydroxy-7-octynoic acid (Dhoya)-containing cyclic depsipeptides, named dudawalamides A-D (1-4), was isolated from a Papua New Guinean field collection of the cyanobacterium Moorea producens using bioassay-guided and spectroscopic approaches. The planar structures of dudawalamides A-D were determined by a combination of 1D and 2D NMR experiments and MS analysis, whereas the absolute configurations were determined by X-ray crystallography, modified Marfey's analysis, chiral-phase GCMS, and chiral-phase HPLC. Dudawalamides A-D possess a broad spectrum of antiparasitic activity with minimal mammalian cell cytotoxicity. Comparative analysis of the Dhoya-containing class of lipopeptides reveals intriguing structure-activity relationship features of these NRPS-PKS-derived metabolites and their derivatives.

Two new 14-membered cyclopeptide alkaloids from Zizyphus xylopyra

The phytochemical investigation of the bark of Zizyphus xylopyra resulted in the isolation of two new 14-membered ring cyclopeptide alkaloids, xylopyrine-G and xylopyrine H. Their structures have been established by chemical and spectral evidences.