75813
N-Benzoyl-L-leucine
≥99.0%
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About This Item
Empirical Formula (Hill Notation):
C13H17NO3
CAS Number:
Molecular Weight:
235.28
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2055078
assay
≥99.0%
form
powder
optical activity
[α]20/D −10.0±1°, c = 1% in methanol
reaction suitability
reaction type: C-H Activation, reaction type: solution phase peptide synthesis, reagent type: ligand
reaction type: Peptide Synthesis
solubility
methanol: 50 mg/mL, clear, colorless
application(s)
peptide synthesis
functional group
amine, carboxylic acid
SMILES string
CC(C)C[C@H](NC(=O)c1ccccc1)C(O)=O
InChI
1S/C13H17NO3/c1-9(2)8-11(13(16)17)14-12(15)10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3,(H,14,15)(H,16,17)/t11-/m0/s1
InChI key
POLGZPYHEPOBFG-NSHDSACASA-N
Other Notes
Employed in the Young test to assess the amount of racemization in peptide coupling[1]
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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M.W. Williams et al.
Journal of the Chemical Society, 881-881 (1963)
2-Mercaptopyridone 1-Oxide-Based Uronium Salts: New Peptide Coupling Reagents(1)(,)(2).
Miguel A. Bailén et al.
The Journal of organic chemistry, 64(24), 8936-8939 (2001-10-25)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 75813-5G | 04061832642963 |