168292-71-5

Basic information

• Product Name: N-BENZYL-N-METHYL-D-ALANINE METHYL ESTER HYDROCHLORIDE
• Synonyms: N-BENZYL-N-METHYL-D-ALANINE METHYL ESTER HYDROCHLORIDE;BZL,ME-D-ALA-OME HCL;BZL-N-ME-D-ALA-OME HCL
• CAS NO: 168292-71-5
• Molecular Formula: C12H18ClNO2
• Molecular Weight: 243.73
• Mol File: 168292-71-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 265.7±23.0 °C(Predicted)
• Appearance: /
• Density: 1.039±0.06 g/cm3(Predicted)
• PKA: 6.34±0.50(Predicted)
• CAS DataBase Reference: N-BENZYL-N-METHYL-D-ALANINE METHYL ESTER HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-BENZYL-N-METHYL-D-ALANINE METHYL ESTER HYDROCHLORIDE(168292-71-5)
• EPA Substance Registry System: N-BENZYL-N-METHYL-D-ALANINE METHYL ESTER HYDROCHLORIDE(168292-71-5)

Safety Data

• Hazardous Substances Data: 168292-71-5(Hazardous Substances Data)

Upstream product

• 124-41-4 sodium methylate 
• 120571-58-6 N-benzyl D-alanine methyl ester 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 103-67-3 benzyl-methyl-amine 
• 157163-04-7 tert-Butyl (4S)-3-<(2R)-2-(N-benzylamino)propionyl>-1-methyl-2-oxoimidazolidine-4-carboxylate 
• 168292-68-0 (4S)-3-<(2R)-2-(N-Benzylamino)propionyl>-4-(tert-butoxymethyl)-1-methyl-2-oxoimidazolidine 
• 100-52-7 benzaldehyde 
• 50-00-0 formaldehyd 
• 159721-22-9 N-benzyl-alanine methyl ester 
• 40216-71-5 methyl 2-(benzylideneamino)propanoate 
• 31022-10-3 N-benzyl-L-alanine methyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 52060-77-2 H-MeAla-OMe 

Relevant articles and documents

THERAPEUTIC COMPOUNDS

The present invention relates to compounds that are antagonists of the orexin-1 receptor. The compounds have the structural formula (I) defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of diseases or disorders associated with orexin-1 receptor activity.

L-alanine-derived chiral ligands for asymmetric addition of diethylzinc to aldehydes

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Photoinduced electron transfer (PET) promoted oxidative activation of 1- (N-benzyl-N-methylglycyl)-(S)-prolinol: Development of novel strategies towards enantioselective syntheses of α-amino acids, their N-methyl derivatives and α-hydroxy acids employing

PET activation of 1-(N-benzyl-N-methylglycyl)-(S)-prolinol (1) in dry acetonitrile, utilizing 1,4-dicyanonaphthalene (DCN) as a light-harvesting electron-acceptor and methyl viologen (MV++) as an electron-transfer mediator, leads to the formati