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Z-L-Orn(Boc)-OH

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:Cbz-Orn(Boc)-OH
CAS:7733-29-1
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:(S)-2-(((Benzyloxy)carbonyl)amino)-5-((tert-butoxycarbonyl)amino)pentanoic acid
CAS:7733-29-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-36754
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:n-cbz-n'-boc-l-ornithine
CAS:7733-29-1
Purity:99% Package:1kg
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Products Intro: Product Name:Z-ORN(BOC)-OH
CAS:7733-29-1
Purity:98% HPLC Package:1KG;1USD
Company Name: GL Biochem(Binhai) Ltd.
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Products Intro: Product Name:Z-Orn(Boc)-OH
CAS:7733-29-1
Purity:98%; 99% Package:50G,1Kg, 50Kg

Z-L-Orn(Boc)-OH manufacturers

  • Z-ORN(BOC)-OH
  • Z-ORN(BOC)-OH pictures
  • $1.00
  • 2020-03-05
  • CAS:7733-29-1
  • Min. Order: 1KG
  • Purity: 98% HPLC
  • Supply Ability: 10 tons
Z-L-Orn(Boc)-OH Basic information
Product Name:Z-L-Orn(Boc)-OH
Synonyms:N-ALPHA-BENZYLOXYCARBONYL-N-DELTA-BOC-L-ORNITHINE;N-ALPHA-BENZYLOXYCARBONYL-N-DELTA-T-BUTYLOXYCARBONYL-L-ORNITHINE;N-ALPHA-BENZYLOXYCARBONYL-N-DELTA-TERT-BUTYLOXYCARBONYL-L-ORNITHINE;N-ALPHA-CARBOBENZOXY,N-DELTA-T-BUTOXYCARBONYL-L-ORNITHINE;N-ALPHA-CBZ-N-DELTA-T-BOC-L-ORNITHINE;Z-N-S-BOC-L-ORNITHINE;Z-N-DELTA-BOC-L-ORNITHINE;Z-ORN(BOC)-OH
CAS:7733-29-1
MF:C18H26N2O6
MW:366.41
EINECS:1592732-453-0
Product Categories:Ornithine [Org];Amino Acid Derivatives
Mol File:7733-29-1.mol
Z-L-Orn(Boc)-OH Structure
Z-L-Orn(Boc)-OH Chemical Properties
Melting point 97-103℃
Boiling point 579.1±50.0 °C(Predicted)
density 1.193±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka3.94±0.21(Predicted)
form Solid
AppearanceWhite to off-white Solid
CAS DataBase Reference7733-29-1
Safety Information
MSDS Information
Z-L-Orn(Boc)-OH Usage And Synthesis
Synthesis
N-δ-Boc-L-Ornithine

13650-49-2

Benzyl chloroformate

501-53-1

Z-ORN(BOC)-OH

7733-29-1

To a stirred solution of δ-Boc-L-ornithine (0.5 g, 2.15 mmol, 1 eq.) dissolved in 5% aqueous NaHCO3 (30 mL) was slowly added benzyl chloroformate (0.4 mL, 2.80 mmol, 1.3 eq.) at room temperature. The reaction mixture was stirred continuously for 12 hours at room temperature. Upon completion of the reaction, extraction was performed by adding ether (20 mL) to remove unreacted benzyl chloroformate. The aqueous phase was adjusted to pH 1 with aqueous 6N hydrochloric acid and subsequently extracted with dichloromethane (50 mL x 3). The organic phases were combined, dried with anhydrous MgSO4, filtered and concentrated under reduced pressure to afford the target compound N-benzyloxycarbonyl-N'-tert-butoxycarbonyl-L-ornithine (Compound 13) as a colorless solid (0.71 g) in 90% yield.

References[1] European Journal of Medicinal Chemistry, 2018, vol. 149, p. 122 - 128
[2] Helvetica chimica acta, 1966, vol. 49, # 3, p. 1013 - 1022
[3] Patent: US2004/6062, 2004, A1. Location in patent: Page/Page column 42
[4] FEBS Journal, 2013, vol. 280, # 8, p. 1807 - 1817
Z-L-Orn(Boc)-OH Preparation Products And Raw materials
Raw materialsN-δ-Boc-L-Ornithine-->Benzyl chloroformate-->Sodium bicarbonate
Tag:Z-L-Orn(Boc)-OH(7733-29-1) Related Product Information
Z-N-Methyl-D-valine ZOTAROLIMUS ZPCK Z-NVA-OH ZM 39923 HYDROCHLORIDE ZM 336372 Z-NLE-OH Z-Orn(Boc)-ONP Z-ORN(Z)-OH Z-ORN-OH Z-ORN(FMOC)-OH L(+)-N-CBZ-ORNITHINE HYDROCHLORIDE Z-ORN(BOC)-OH DCHA Z-Orn(Z)-OH.DCHA Nα-Z-Nδ-Boc-L-ornithine L-Ornithine Fmoc-Orn(Boc)-OH BOC-ORN(BOC)-OH