1. chem960
  2. 35737-15-6
Names and Identifiers
  • N(alpha)-Fmoc-L-tryptophan
  • N(alpha)-9-Fluorenylmethoxycarbonyl-L-tryptophan
  • Fmoc-Trp-OH
  • Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tryptophan
  • 9-FLUORENYLMETHOXYCARBONYL-L-TRYPTOPHAN
  • Fmoc-L-Trp-OH
  • H-Ser(Bzl)-OH∙HCl
  • Nalpha-FMOC-L-Tryptophan
  • N-Fmoc-L-Tryptophan
  • Nα-Fmoc-L-tryptophan
  • PARAGOS 300355
  • FMOC-L-TRP
  • Fmoc-L-tryptophan
  • FMOC-L-TRYPTOPHAN-OH
  • FMOC-TRP
  • FMOC-TRYPTOPHAN
  • L-TRYPTOPHAN-N-FMOC
  • Nalpha-FMOC-L-Trypto
  • N-Fmoc-L-Trp-OH
  • Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tryptophan
  • Nalpha-(9-Fluorenylmethoxycarbonyl)-L-tryptophan
  • L-Tryptophan, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
  • MGHMWKZOLAAOTD-DEOSSOPVSA-N
  • C26H22N2O4
  • (s)-2-(((9h-fluoren-9-yl)methoxy)carbonylamino)-3-(1h-indol-3-yl)propanoic acid
  • (S)-2-((((9H-FLUOREN-9-YL)METHOXY)CARBONYL)AMINO)-3-(1H-INDOL-3-YL)PROPANOIC ACID
  • (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)-propionic acid
  • (2R)-2-{[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]AM
  • PubChem10045
  • N-
  • A-Fmoc-L-tryptophan
  • MLS001359854
  • KSC223A7J
  • HMS3030J08
  • BDBM50043810
  • Fmoc-L-tryptophan(35737-15-6)
  • Fmoc-L-tryptophan:(35737-15-6)
  • (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)propanoic acid
  • (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(1H-indol-3-yl)propanoic acid
  • EN300-81250
  • Fmoc-L-Trp-OH Fmoc-L-tryptophan
  • J-300269
  • Fmoc-Trp-OH, >=97.0% (HPLC)
  • Q-101610
  • MFCD00037126
  • 35737-15-6
  • SCHEMBL119372
  • F0307
  • (((9H-Fluoren-9-yl)methoxy)carbonyl)-L-tryptophan
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]tryptophan #
  • AC-8601
  • (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)propanoate
  • Fmoc-Trp-OH
  • NCGC00247299-01
  • AKOS012535969
  • AKOS015924240
  • A822965
  • M03374
  • AM82281
  • AS-12714
  • SMR001224401
  • N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-tryptophan (Fmoc-L-Trp-OH)
  • CS-W011637
  • NS00057859
  • CHEMBL292051
  • Fmoc-Trp-OH,98%
  • MDL:MFCD00037126
  • InChIKey:MGHMWKZOLAAOTD-DEOSSOPVSA-N
  • Inchi:1S/C26H22N2O4/c29-25(30)24(13-16-14-27-23-12-6-5-7-17(16)23)28-26(31)32-15-22-20-10-3-1-8-18(20)19-9-2-4-11-21(19)22/h1-12,14,22,24,27H,13,15H2,(H,28,31)(H,29,30)/t24-/m0/s1
  • SMILES:O(C(N([H])[C@]([H])(C(=O)O[H])C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12)=O)C([H])([H])C1([H])C2=C([H])C([H])=C([H])C([H])=C2C2=C([H])C([H])=C([H])C([H])=C12
  • BRN:4216624
Chemical and Physical Properties

Computed Properties

  • Exact Mass: 426.5g/mol
  • Surface Charge: 0
  • XLogP3: 4.1
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Rotatable Bond Count: 7
  • Monoisotopic Mass: 426.157957g/mol
  • Monoisotopic Mass: 426.157957g/mol
  • Topological Polar Surface Area: 91.4Ų
  • Heavy Atom Count: 32
  • Complexity: 663
  • Isotope Atom Count: 0
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Covalently-Bonded Unit Count: 1
  • Surface Charge: 0

Experimental Properties

  • LogP: 5.09320
  • PSA: 91.42000
  • Refractive Index: -28.5 ° (C=1, DMF)
  • Boiling Point: 711.9°C at 760 mmHg
  • Melting Point: 185.0 to 188.0 deg-C
  • Flash Point: 384.3℃
  • Color/Form: powder
  • Solubility: Not determined
  • Specific Rotation: -29 º (c=1,DMF)
  • Optical Activity: [α]20/D −29±1°, c = 1% in DMF
  • Density: 1.2501 (rough estimate)
Security Information
  • WGK Germany:3
  • Safety Term:S22;S24/25
  • Safety Instruction:S22-S24/25
  • Risk Phrases:R36/37/38
  • Tehlikeli mal işareti: Xi Xi
  • Hazardous Material transportation number:NONH for all modes of transport
  • Hazard Statement:H302-H315-H319-H335
  • Warning Statement:P261-P305+P351+P338
  • Storage Condition:2-8°C
  • Hazard Category Code:36/37/38
  • Signal Word:Warning
Synthetic Circuit

Synthetic Circuit 1

Reaction Conditions
Reference
Preparation of an O-[2-(methacryloyloxy)-ethylcarbamoyl]-10,11-dihydroquinidine-silica hybrid monolithic column for the enantioseparation of amino acids by nano-liquid chromatography
Xu, Dongsheng; et al, Journal of Chromatography A, 2019, 1593, 63-72

Synthetic Circuit 2

Reaction Conditions
Reference
2-Acyl-dimedones as UV-active protective agents for chiral amino acids: enantiomer separations of the derivatives on chiral anion exchangers
Wernisch, Stefanie; et al, Analytical and Bioanalytical Chemistry, 2013, 405(25), 8011-8026

Synthetic Circuit 3

Reaction Conditions
Reference
Chiral separation of acidic compounds using an O-9-(tert-butylcarbamoyl)quinidine functionalized monolith in micro-liquid chromatography
Wang, Qiqin; et al, Journal of Chromatography A, 2016, 1444, 64-73
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