Fmoc-Ile-OH

Fmoc-Ile-OH Basic information
Product Name:Fmoc-Ile-OH
Synonyms:Fmoc-Ile-OH >=98.0% (T);N-FMOC-L-ISOLEUCINE;N-FMOC-ILE-OH;Fmoc-(2S,3S)-2-amino-3-methylpentanoic acid;Fmoc-L-isoleucine≥ 99% (HPLC);Fmoc-lle-OH;L-Isoleucine, FMOC protected;N-FMOC-ILE-OH ( N-FMOC-L-ISOLEUCINE)
CAS:71989-23-6
MF:C21H23NO4
MW:353.41
EINECS:276-255-9
Product Categories:Isoleucine [Ile, I];Fmoc-Amino Acids and Derivatives;Amino Acids (N-Protected);Biochemistry;Fmoc-Amino Acids;Fmoc-Amino acid series;Protected Amino Acids;Fluorenes, Flurenones;AMINOACIDS DERIVATIVES;Amino Acids
Mol File:71989-23-6.mol
Fmoc-Ile-OH Structure
Fmoc-Ile-OH Chemical Properties
Melting point 145-147 °C(lit.)
alpha -12 º (c=1,DMF)
Boiling point 486.83°C (rough estimate)
density 1.2107 (rough estimate)
refractive index -12 ° (C=1, DMF)
storage temp. 2-8°C
solubility Soluble in methanol (very faint turbidity).
pka3.92±0.22(Predicted)
form Fine Crystalline Powder
color White
optical activity[α]20/D 12±1°, c = 1% in DMF
BRN 4716717
InChIInChI=1S/C21H23NO4/c1-3-13(2)19(20(23)24)22-21(25)26-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,13,18-19H,3,12H2,1-2H3,(H,22,25)(H,23,24)/t13-,19-/m0/s1
InChIKeyQXVFEIPAZSXRGM-DJJJIMSYSA-N
SMILESC(O)(=O)[C@H]([C@@H](C)CC)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O
CAS DataBase Reference71989-23-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36/37/39-27-26
WGK Germany 3
Hazard Note Irritant
HS Code 2924 29 70
MSDS Information
Fmoc-Ile-OH Usage And Synthesis
Description Fmoc-Ile-OH is an isoleucine derivative. It is white fine crystalline powder and belong to Fmoc materials. Fmoc-Leu-OH forms flower-like morphology at both low and high concentration under room temperature which changes to small tube-like structure on heating[1].
Chemical Propertieswhite fine crystalline powder
UsesN-Fmoc-L-isoleucine is an unnatural amino acid used for peptidomimetics. It is also used as a pharmaceutical intermediate.
General DescriptionThe product number for this product was previously 04-12-1024.

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References[1] N. Gour, B. Koshti, S. Naskar, V. Kshtriya, H. Narode, Self-assembled Structures Formed by Fmoc modified aliphatic amino acids, ChemRxiv, 2021.
1,1'-Carbonyldiimidazole (2R,3R)-2-Amino-3-methylpentanoic acid Fmoc-N-methyl-L-isoleucine N-ALPHA-FMOC-L-ISOLEUCINE PENTAFLUOROPHENYL ESTER,FMOC-L-ISOLEUCINE PENTAFLUOROPHENYL ESTER FMOC-L-ISOLEUCINE N-HYDROXYSUCCINIMIDE ESTER,FMOC-L-ISOLEUCINE HYDROXYSUCCINIMIDE ESTER,FMOC-L-ISOLEUCINE HYDROXYSUCCINIMIDESTER N-alpha-FMOC-Nepsilon-BOC-L-Lysine L-Isoleucine PYRAZOPHOS Fmoc-Aib-OH fmoc-L-isoleucine N-carboxy anhydride ALTRENOGEST Isoleucine FMOC-CHG-OH FMOC-L-ISOLEUCINE-15N AMINO ACIDS L-Leucine Fmoc N-CARBOBENZOXY-DL-LEUCINE

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