47633

Fmoc-Leu-OH

≥97.0%

Manufacturer: Sigma Aldrich

CAS Number: 35661-60-0

Synonym(S): N-(9-Fluorenylmethoxycarbonyl)-L-leucine, Fmoc-L-leucine

Select a Size

Pack Size SKU Availability Price
5 G 47633-5-G In Stock ₹ 3,810.40
50 G 47633-50-G In Stock ₹ 8,497.63
250 G 47633-250-G In Stock ₹ 16,215.85

47633 - 5 G

₹ 3,810.40

In Stock

Quantity

1

Base Price: ₹ 3,810.40

GST (18%): ₹ 685.872

Total Price: ₹ 4,496.272

Quality Level

100

Assay

≥97.0%

optical activity

[α]20/D −25±2°, c = 1% in DMF

reaction suitability

reaction type: C-H Activationreaction type: Fmoc solid-phase peptide synthesisreagent type: ligandreaction type: Peptide Synthesis

mp

152-156 °C (lit.)152-156 °C

application(s)

peptide synthesis

functional group

Fmocaminecarboxylic acid

storage temp.

2-8°C

SMILES string

CC(C)C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/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

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Description

  • Application: Fmoc-Leu-OH can be used as a reactant to synthesize:Various oligopeptides by reacting with functionalized α-amino acid hydrochloride salts.[1]A cyclic depsipeptide sansalvamide A, a natural product found in marine fungus.[2]Streptocidin A−D, decapeptide antibiotics naturally found in Streptomyces sp. Tü 6071.[3]Coumaroyl dipeptide amide that can be used for cosmetic applications.[4]
  • Biochem/physiol Actions: PPARγ ligand that induces insulin sensitization, but not adipogenesis.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves