Fmoc-Ile-OH

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Names

[ CAS No. ]:
71989-23-6

[ Name ]:
Fmoc-Ile-OH

[Synonym ]:
L-Isoleucine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-isoleucine
N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-isoleucine
EINECS 276-255-9
MFCD00037125
N-(9-Fluorenylmethoxycarbonyl)-L-isoleucine
N-Fmoc-Ile-OH ( N-Fmoc-L-isoleucine)
FMOC-L-Isoleucine
Fmoc-Ile-OH

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
559.8±33.0 °C at 760 mmHg

[ Melting Point ]:
145-147 °C(lit.)

[ Molecular Formula ]:
C21H23NO4

[ Molecular Weight ]:
353.412

[ Flash Point ]:
292.4±25.4 °C

[ Exact Mass ]:
353.162720

[ PSA ]:
75.63000

[ LogP ]:
4.95

[ Vapour Pressure ]:
0.0±1.6 mmHg at 25°C

[ Index of Refraction ]:
1.583

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • L-Isoleucine
  • Fmoc-Osu
  • 9H-Fluoren-9-ylmethyl pentafluorophenyl carbonate
  • 9H-fluoren-9-ylmethyl 2,5-dioxopyrrolidine-1-carboxylate
  • 9-Fluorenylmethyl chloroformate
  • L-Isoleucine hydrochloride

DownStream

  • L-Isoleucine
  • Fmoc-L-Ile-CHN2
  • Fmoc-Ile-OPfp
  • Angiotensin I/II (4-8)
  • Fmoc-Ile-ol
  • fmoc-ile-cl
  • Cecropin A (1-7)-Melittin A (2-9) amide trifluoroacetate salt
  • L-isoleucinamide
  • Fmoc-β-homoisoleucine
  • Endothelin (16-21) trifluoroacetate salt

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Complete ON/OFF photoswitching of the motility of a nanobiomolecular machine.

ACS Nano 8(5) , 4157-65, (2014)

To apply motor proteins as natural nanomolecular machines to transporting systems in nanotechnology, complete temporal control over ON/OFF switching of the motility is necessary. We have studied the p...

Design and synthesis of newN-(fluorenyl-9-methoxycarbonyl) (Fmoc)-dipeptides as anti-inflammatory agents

Eur. J. Med. Chem. 44 , 1933-40, (2009)

Twenty-four new dipeptide analogs ( 1– 24) of aurantiamide acetate were designed, synthesized, and assayed for effects on superoxide anion generation and elastase release by human neutrophils in respo...


More Articles

Related Compounds

  • FMOC-ILE-OH
  • Fmoc-Ile-OH
  • fmoc-ile-oh-15n
  • Fmoc-Ile-OH-13C6,15N
  • N-Fmoc-Ile-OH ( N-Fmoc-L-isoleucine)
  • N-Fmoc-Ile-OH ( N-Fmoc-L-isoleucine)
  • Ethyl 4-[(4,6-dimethylpyrimidin-2-yl)sulfanyl]-3-oxobutanoate
  • 1-(4-Bromophenoxy)-3,3-dimethyl-2-butanone
  • 1-(3-Bromophenoxy)-3,3-dimethylbutan-2-one
  • 1-(1-Naphthalenyl)-2-phenoxyethanone
  • 3-(4-Amino-3-methyl-5-nitro-phenyl)-2-oxo-propionic acid
  • Ethyl 4-[2-(4-morpholinyl)-2-oxoethoxy]benzoate
  • 2-(3-Iodophenoxy)-1-(piperidin-1-yl)ethan-1-one
  • 3-(4-Iodophenoxy)butan-2-one
  • 2-(4-bromo-2-fluorophenoxy)-N,N-dimethylacetamide
  • 2-(4-Bromo-2-fluorophenoxy)-1-(pyrrolidin-1-yl)ethan-1-one
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