Boc-Ala-OH
ALDRICH/15380 - ≥99.0% (TLC)
Synonym: N-(tert-Butoxycarbonyl)-L-alanine; Boc-L-alanine
CAS Number: 15761-38-3
Empirical Formula (Hill Notation): C8H15NO4
Molecular Weight: 189.21
EC Number: 239-847-8
MDL Number: MFCD00037225
Linear Formula: CH3CH[NHCO2C(CH3)3]CO2H
Product Type: Chemical
application(s) | peptide synthesis |
assay | ≥99.0% (TLC) |
functional group | amine |
carboxylic acid | |
InChI | 1S/C8H15NO4/c1-5(6(10)11) |
InChI key | QVHJQCGUWFKTSE-YFKPBYRVSA |
mp | 79-83 °C (lit.) |
optical activity | [α]20/D −25±1°, c = 2% in acetic acid |
Quality Level | 100 |
reaction suitability | reaction type: Boc solid-phase peptide synthesis |
reaction type: C-H Activation | |
reagent type: ligand reaction type: Peptide Synthesis |
|
SMILES string | C[C@H](NC(=O)OC(C)(C)C)C( |
Application: | Boc-Ala-OH can be used: • In the preparation of N-propargylalanine, a key precursor to generate N-(3-aryl)propylated alanine residues. • In the resolution of racemic mixture of 3,3′-bis(benzyloxy)-1,1′- • In the one-pot synthesis of hybrid tripeptidomimetics containing both amide and imide functionalities. |
Packaging: | 5, 25, 100 g in glass bottle |
RIDADR | NONH for all modes of transport |
WGK Germany | WGK 3 |
Flash Point(F) | Not applicable |
Flash Point(C) | Not applicable |
Purity | ≥99.0% (TLC) |
mp | 79-83 °C (lit.) |
UNSPSC | 12352209 |