Fmoc-Leu-OH CAS 35661-60-0

Fmoc-Leu-OH CAS 35661-60-0

N-(9-Fluorenylmethoxycarbonyl)-L-leucine, Fmoc-L-leucine

Fmoc-Leu-OH CAS35661-60-0
CAS:35661-60-0           MW:353.41
Empirical Formula (Hill Notation):C21H23NO4
CAS Number:35661-60-0
Molecular Weight:353.41
Beilstein:2178254
EC Number:252-662-7
MDL number:MFCD00037133
UNSPSC Code:12352209
eCl@ss:32160406
PubChem Substance ID:57651051
NACRES:NA.26

 

Assay≥97.0%
optical activity[α]20/D −25±2°, c = 1% in DMF
reaction suitabilityreaction type: C-H Activation
reaction type: Fmoc solid-phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis
mp152-156 °C (lit.)
152-156 °C
application(s)peptide synthesis
functional groupFmoc
aminecarboxylic acid
storage temp.2-8°C
SMILES stringCC(C)C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI1S/C21H23NO4/c1-13(2)11-19(20(23)24)22-21(25)26-12-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h3-10,13,18-19H,11-12H2,1-2H3,(H,22,25)(H,23,24)/t19-/m0/s1
InChI keyCBPJQFCAFFNICX-IBGZPJMESA-N

 

Application:

Fmoc-Leu-OH can be used as a reactant to synthesize:

Various oligopeptides by reacting with functionalized α-amino acid hydrochloride salts.

A cyclic depsipeptide sansalvamide A, a natural product found in marine fungus.

Streptocidin A−D, decapeptide antibiotics naturally found in Streptomyces sp.

Coumaroyl dipeptide amide that can be used for cosmetic applications.

Biochem/physiol Actions:

PPARγ ligand that induces insulin sensitization, but not adipogenesis.

Application

ORID products are tested extensively in-house and supplied worldwide to the Life Sciences industries.

Company Profile

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