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Merck
CN

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
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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

SMILES string

CC(C)C[C@H](NC(=O)c1ccccc1)C(O)=O

InChI key

POLGZPYHEPOBFG-NSHDSACASA-N

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

Other Notes

Employed in the Young test to assess the amount of racemization in peptide coupling

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)

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