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N5-(aminocarbonyl)-N2-[(phenylmethoxy)carbonyl]-L-ornithine

Basic Information

  • CAS No.: 6692-89-3
  • Purity: 99%
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Details

High quality purity >99% N5-(aminocarbonyl)-N2-[(phenylmethoxy)carbonyl]-L-ornithine 6692-89-3 for sale

  • Molecular Formula: C14H19 N3 O5
  • Molecular Weight: 309.322
  • Vapor Pressure: 8.17E-14mmHg at 25°C 
  • Boiling Point: 569.6°C at 760 mmHg 
  • Flash Point: 298.3°C 
  • PSA： 130.75000 
  • Density: 1.298g/cm3 
  • LogP: 2.29660 

N5-(aminocarbonyl)-N2-[(phenylmethoxy)carbonyl]-L-ornithine(Cas 6692-89-3) Usage

General Description

N5-(aminocarbonyl)-N2-[(phenylmethoxy)carbonyl]-L-ornithine is a chemical compound that belongs to the class of ornithine derivatives. It is a derivative of the amino acid ornithine, which plays a key role in the urea cycle and the biosynthesis of proteins. This specific compound contains a carbonyl group and an amino group, as well as a phenylmethoxy group attached to the N2 position of the ornithine molecule. It may have potential applications in biochemical research or pharmaceutical development, and its properties and biological effects could be of interest for further investigation.

InChI:InChI=1/C14H19N3O5/c15-13(20)16-8-4-7-11(12(18)19)17-14(21)22-9-10-5-2-1-3-6-10/h1-3,5-6,11H,4,7-9H2,(H,17,21)(H,18,19)(H3,15,16,20)/t11-/m0/s1

6692-89-3 Relevant articles

Improved Methodology for the Synthesis of a Cathepsin B Cleavable Dipeptide Linker, Widely Used in Antibody-Drug Conjugate Research

Mondal, Deboprosad,Ford, Jacob,Pinney, Kevin G.

supporting information, p. 3594 - 3599 (2018/09/11)

Antibody-drug conjugates (ADCs) represen...

Urea cycle: Chemical simulation of arginine biosynthesis

Ranganathan,Rathi

, p. 2351 - 2354 (2007/10/02)

We have successfully simulated the salie...

6692-89-3 Process route

N-(Benzyloxycarbonyloxy)succinimide
13139-17-8

N-(Benzyloxycarbonyloxy)succinimide

Citrulline
372-75-8

Citrulline

N<sup>α</sup>-benzyloxy-carbonyl-L-citrulline
6692-89-3,13594-52-0

Nα -benzyloxy-carbonyl-L-citrulline

Conditions
Conditions Yield
Citrulline; With sodium hydrogencarbonate; In water; at 20 ℃; for 1h;
N-(Benzyloxycarbonyloxy)succinimide; In 1,2-dimethoxyethane; water; at 20 ℃;
100%
Citrulline
372-75-8

Citrulline

N<sup>α</sup>-benzyloxy-carbonyl-L-citrulline
6692-89-3,13594-52-0

Nα -benzyloxy-carbonyl-L-citrulline

Conditions
Conditions Yield
With sodium hydroxide; benzyl chloroformate; toluene;

6692-89-3 Upstream products

  • 372-75-8
    372-75-8

    Citrulline

  • 13139-17-8
    13139-17-8

    N-(Benzyloxycarbonyloxy)succinimide

  • 372-75-8
    372-75-8

    2-Amino-5-ureido-pentanoic acid

  • 501-53-1
    501-53-1

    benzyl chloroformate

6692-89-3 Downstream products

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    122702-26-5

    N -(N 2 -benzyloxycarbonyl-N 5 -carbamoyl-L-ornithyl)-L-glutamic acid dibenzyl ester

  • 89499-13-8
    89499-13-8

    methyl Nα -benzyloxycarbonyl-L-citrullinate

  • 587-90-6
    587-90-6

    bis-N,N'-(4-nitrophenyl)urea

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    38150-56-0

    3-(benzyloxycarbonylamido)-piperidin-2-one

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