93709-64-9

Basic information

• Product Name: L-Alanine, N-(4-methoxybenzoyl)-
• Synonyms: p-Methoxybenzoyl-L-alanine;N-(4-Methoxybenzoyl)-L-alanine
• CAS NO: 93709-64-9
• Molecular Formula: C11H13NO4
• Molecular Weight: 223.229
• Mol File: 93709-64-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 457.9±30.0 °C (760 mmHg)
• Density: 1.227±0.06 g/cm3 (20 °C, 760 mmHg)
• CAS DataBase Reference: L-Alanine, N-(4-methoxybenzoyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, N-(4-methoxybenzoyl)-(93709-64-9)
• EPA Substance Registry System: L-Alanine, N-(4-methoxybenzoyl)-(93709-64-9)

Safety Data

• Hazardous Substances Data: 93709-64-9(Hazardous Substances Data)

Upstream product

• 100-09-4 4-methoxybenzoic acid 
• 56-41-7 L-alanin 
• 132353-25-4 2-(4-methoxybenzoyloxy)-4,6-dimethoxy-1,3,5-triazine 
• 125700-05-2 (S)-methyl (4-methoxybenzoyl)alaninate 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 99553-79-4 2-(4-methoxyphenyl)-4-methyl-5-oxo-4,5-dihydrooxazole 
• 125700-05-2 (S)-methyl (4-methoxybenzoyl)alaninate 
• 1208130-64-6 N-((S)-1-((S)-1-(hydroxyamino)-5-(3-nitroguanidino)-1-oxopentan-2-ylamino)-1-oxopropan-2-yl)-4-methoxybenzamide 
• 56-41-7 L-alanin 
• 100-09-4 4-methoxybenzoic acid 
• 93709-70-7 4-MeOBz-D-Ala-L-PheOMe 
• 93709-94-5 4-MeOBz-D-Ala-L-PheOMe 
• 93709-71-8 4-MeOBz-L-Ala-L-ValOMe 
• 93709-95-6 4-MeOBz-D-Ala-L-ValOMe 
• 93709-69-4 4-MeOBz-L-Ala-L-AlaOMe 
• 93709-93-4 4-MeOBz-D-Ala-L-AlaOMe 

Relevant articles and documents

Development of a method for the synthesis of 2,4,5-trisubstituted oxazoles composed of carboxylic acid, amino acid, and boronic acid

A novel method for the synthesis of trisubstituted oxazoles via a one-pot oxazole synthesis/Suzuki–Miyaura coupling sequence has been developed. One-pot formation of 5-(triazinyloxy)oxazoles using carboxylic acids, amino acids and a dehydrative condensing reagent, DMT-MM, followed by Ni-catalyzed Suzuki–Miyaura coupling with boronic acids provided the corresponding 2,4,5-trisubstituted oxazoles in good yields.

Design, synthesis and primary activity assay of bi- or tri-peptide analogues with the scaffold l-arginine as amino-peptidase N/CD13 inhibitors

A series of bi- or tri-peptide analogues with the scaffold l-arginine were designed, synthesized and evaluated for their inhibitory activities against amino-peptidase N (APN) and metalloproteinase-2 (MMP-2). The primary activity assay showed that all the compounds exhibited higher inhibitory activities against APN than MMP-2. Within this series, compounds C6 and C7 (IC50 = 4.2 and 4.3 μM) showed comparable APN inhibitory activities with the positive control bestatin (IC50 = 3.8 μM).

N-TERMINAL SUBSTITUENT AND SIDE-CHAIN INFLUENCES ON THE CHEMICAL SHIFTS OF PROTONS IN MODEL DIPEPTIDE SYSTEMS

(1)H Chemical shift values of ester methyls in model dipeptide esters have been shown to be sensitive to (a) the nature and configuration of the constituent amino acids and (b) the spatial distance between the N-terminal aryl group and the ester protons.C