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Fmoc-Dab-OH HCl

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Fmoc-Dab-OH HCl manufacturers

  • FMOC-DAB-OH HCL
  • FMOC-DAB-OH HCL pictures
  • 2026-09-20
  • CAS:161420-87-7
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 2000
  • FMOC-DAB-OH HCL
  • FMOC-DAB-OH HCL pictures
  • $1.00
  • 2019-07-06
  • CAS:161420-87-7
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1kg,5kg,100kg
Fmoc-Dab-OH HCl Basic information
Product Name:Fmoc-Dab-OH HCl
Synonyms:FMOC-L-ALPHA,GAMMA-DIAMINOBUTYRIC ACID;FMOC-ALPHA,GAMMA-DIAMINOBUTYRIC ACID;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-2,4-DIAMINOBUTYRIC ACID;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ALPHA, GAMMA-DIAMINOBUTYRIC ACID;N-ALPHA-FMOC-L-ALPHA,GAMMA-DIAMINOBUTYRIC ACID;N-α-Fmoc-L-2,4-diaminobutyric acid;N-ALPHA-(9-FLUOROENYLMETHYLOXYCARBONYL)-L-2,4-DIAMINOBUTYRIC ACID;FMOC-DAB-OH . HCI
CAS:161420-87-7
MF:C19H20N2O4
MW:340.37
EINECS:
Product Categories:
Mol File:161420-87-7.mol
Fmoc-Dab-OH HCl Structure
Fmoc-Dab-OH HCl Chemical Properties
Melting point 169.5-171.7 °C
Boiling point 593.7±50.0 °C(Predicted)
density 1.294±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
form Powder
pka3.52±0.10(Predicted)
color White to off-white
Safety Information
HazardClass IRRITANT
MSDS Information
Fmoc-Dab-OH HCl Usage And Synthesis
Synthesis
Nalpha-FMOC-L-Glutamine

71989-20-3

FMOC-DAB-OH HCL

161420-87-7

The general procedure for the synthesis of Fmoc-L-2,4-diaminobutyric acid (Fmoc-Dab-OH) from (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-amino-5-oxopentanoic acid (Fmoc-Gln-OH) was as follows: A. 100 g (271.5 mmol) of Fmoc-Gln-OH was suspended in 2 L of a solvent mixture consisting of ethyl acetate, acetonitrile and water in the ratio of 2:1:1 by volume. 105.1 g (325.9 mmol) of diisopropylethylamine (DIPA) was slowly added at 20-30 °C and the reaction lasted for 72 hours. Upon completion of the reaction, 80 g of Fmoc-Dab-OH was obtained after post-processing in 86.5% yield. The product was analyzed by high performance liquid chromatography (HPLC) showing a purity of 99.6%, and its structural correctness was confirmed by infrared spectroscopy (IR) and nuclear magnetic resonance (NMR), and the relevant spectra are shown in Figures 1 and 2.

References[1] Bulletin of the Chemical Society of Japan, 2004, vol. 77, # 10, p. 1915 - 1924
[2] Patent: CN105348147, 2016, A. Location in patent: Paragraph 0014
[3] Synlett, 2011, # 13, p. 1917 - 1919
[4] Journal of Peptide Science, 2017, vol. 23, # 3, p. 202 - 214
[5] European Journal of Medicinal Chemistry, 1995, vol. 30, # 2, p. 115 - 122
Fmoc-Dab-OH HCl Preparation Products And Raw materials
Raw materialsNalpha-FMOC-L-Glutamine-->Ethyl acetate-->Acetonitrile-->(Diacetoxyiodo)benzene-->Water
Preparation ProductsFmoc-Dab(Boc)-OH
Tag:Fmoc-Dab-OH HCl(161420-87-7) Related Product Information
Fmoc-Asn(Trt)-OPfp Nalpha-FMOC-L-Asparagine Fmoc-Asn(Trt)-OH 2,4-Diamino-butyric acid Fmoc-Dab(Boc)-OH 4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester Fmoc-Dab(ivDde)-OH Fmoc-Dab(aloc)-OH Fmoc-Dab-OH HCl Fmoc-Asn(AC3ACNH-beta-Glc)-OH Fmoc-Asn(Dod)-OH N-α-Fmoc-N-γ-trityl-L-asparagine N-carboxyanhydride Fmoc-Asn-ONp Fmoc-Asn-OPfp Fmoc-Asn(Tmob)-OH Fmoc-Dab(Fmoc)-OH Fmoc-Asn(Mtt)-OH Fmoc-Asn(Mtt)-OPfp