118553-99-4

Basic information

• Product Name: H-Orn(2-Cl-Z)-OH
• Synonyms: N-DELTA-(2-CHLOROBENZYLOXYCARBONYL)-L-ORNITHINE;N-DELTA-2-CHLORO-Z-L-ORNITHINE;H-ORN(2-CL-Z)-OH;N'-(2-Chlorobenzyloxycarbonyl)-L-ornithine;H-L-Orn(2-Cl-Z)-OH;(S)-2-amino-5-((2-chlorobenzyloxy)carbonylamino)pentanoic acid;N5-(2-Chlorobenzyloxycarbonyl)-L-ornithine;L-Orn(2-Cl-Z)-OH
• CAS NO: 118553-99-4
• Molecular Formula: C13H17ClN2O4
• Molecular Weight: 300.74
• Product Categories: Amino Acid Derivatives;Amino Acids;Amino Acids and Derivatives;Amino Acids and Derivatives
• Mol File: 118553-99-4.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 516.7 °C at 760 mmHg
• Flash Point: 266.3 °C
• Appearance: /
• Density: 1.32 g/cm³
• Vapor Pressure: 1.67E-11mmHg at 25°C
• Refractive Index: 1.566
• Storage Temp.: Store at 0°C
• PKA: 2.51±0.24(Predicted)
• CAS DataBase Reference: H-Orn(2-Cl-Z)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-Orn(2-Cl-Z)-OH(118553-99-4)
• EPA Substance Registry System: H-Orn(2-Cl-Z)-OH(118553-99-4)

Safety Data

• Hazardous Substances Data: 118553-99-4(Hazardous Substances Data)

Usage

Description

H-Orn(2-Cl-Z)-OH, also known as (2S)-2-Azaniumyl-5-[(2-chlorophenyl)methoxycarbonylamino]pentanoate, is an organic compound with off-white powder form. It is characterized by its chemical structure that includes an azaniumyl group, a chlorophenylmethoxycarbonylamino group, and a pentanoate chain. H-Orn(2-Cl-Z)-OH is notable for its potential applications in various fields due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
H-Orn(2-Cl-Z)-OH is used as a reactant in peptide synthesis for the development of new pharmaceutical compounds. Its unique structure allows for the creation of diverse peptide sequences with potential therapeutic applications.
Used in Chemical Research:
As a chemical with distinct properties, H-Orn(2-Cl-Z)-OH can be utilized in research and development for understanding the behavior of similar compounds and their interactions with other molecules. This can lead to advancements in various chemical and material science applications.
Used in Biochemical Applications:
Due to its potential for peptide synthesis, H-Orn(2-Cl-Z)-OH may also find use in the field of biochemistry, where it could be employed in the design and synthesis of bioactive peptides for various biological studies and potential therapeutic uses.

InChI:InChI=1/C13H17ClN2O4/c14-10-5-2-1-4-9(10)8-20-13(19)16-7-3-6-11(15)12(17)18/h1-2,4-5,11H,3,6-8,15H2,(H,16,19)(H,17,18)/t11-/m0/s1