2706-38-9

Basic information

• Product Name: Z-LEU-GLY-OH
• Synonyms: N-CBZ-L-LEUCYL-GLYCINE;N-CBZ-LEUCYL-GLYCINE;N-CBZ-LEU-GLY-OH;N-CARBOBENZOXY-L-LEUCYLGLYCINE;N-BENZYLOXYCARBONYL-L-LEUCYLGLYCINE;Z-LEU-GLY-OH;Z-LEU-GLY;Z-L-LEUCYL-GLYCINE
• CAS NO: 2706-38-9
• Molecular Formula: C₁₆H₂₂N₂O₅
• Molecular Weight: 322.36
• EINECS: 220-294-6
• Product Categories: Amino Acid Derivatives
• Mol File: 2706-38-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 582 °C at 760 mmHg
• Flash Point: 305.8 °C
• Appearance: /
• Density: 1.203 g/cm³
• Vapor Pressure: 2.17E-14mmHg at 25°C
• Refractive Index: 1.534
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Z-LEU-GLY-OH(CAS DataBase Reference)
• NIST Chemistry Reference: Z-LEU-GLY-OH(2706-38-9)
• EPA Substance Registry System: Z-LEU-GLY-OH(2706-38-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 2706-38-9(Hazardous Substances Data)

Usage

General Description

Z-LEU-GLY-OH is a chemical compound consisting of the amino acids leucine and glycine. It is commonly used as a reagent in peptide synthesis and as a building block for creating peptide chains. The "Z" in the name indicates that the carboxyl group of the leucine residue is protected with a benzyl group, preventing unwanted reactions during peptide synthesis. Z-LEU-GLY-OH has applications in the pharmaceutical and biotechnology industries for the development of peptide-based drugs and research into protein structure and function. Its specific properties make it valuable in the creation and study of peptides with various biological and therapeutic activities.

InChI:InChI=1/C16H22N2O5/c1-11(2)8-13(15(21)17-9-14(19)20)18-16(22)23-10-12-6-4-3-5-7-12/h3-7,11,13H,8-10H2,1-2H3,(H,17,21)(H,18,22)(H,19,20)/t13-/m0/s1

Upstream product

• 2867-06-3 Benzyloxycarbonylleucyl-glycine ethyl ester 
• 686-50-0 L-leucyl-glycine 
• 501-53-1 benzyl chloroformate 
• 5084-98-0 methyl N-benzyloxycarbonyl-L-leucylglicynate 
• 1738-87-0 Z-Leu-ONp 
• 6216-61-1 (S)-(-)-N-(benzyloxycarbonyl)leucinol 
• 7533-40-6 (S)-2-amino-4-methylpentan-1-ol 
• 2018-66-8 Z-Leu-OH 
• 56-40-6 glycine 
• 1738-89-2 Benzyloxycarbonyl-L-leucyl-glycin-benzylester 
• 27461-77-4 N-benzyloxycarbonyl-L-leucylaminoethanol 
• 102156-97-8 N-benzyloxycarbonyl-L-thioleucine S-phenyl ester 
• 4091-51-4 N-Benzyloxycarbonyl-L-leucin- 
• 19912-26-6 Z-L-Leu-Gly-ODAE 

Downstream Products

• 114225-04-6 N-(N-benzyloxycarbonyl-L-leucyl)-thioglycine S-(4-nitro-phenyl ester) 
• 20806-85-3 N-[N-(N-benzyloxycarbonyl-L-leucyl)-glycyl]-glycine ethyl ester 
• 92911-77-8 N-{N-[N-(N-benzyloxycarbonyl-L-leucyl)-glycyl]-glycyl}-glycine ethyl ester 
• 686-50-0 L-leucyl-glycine 
• 59179-78-1 2-benzoyl-4-chloro-N^α-<(benzyloxycarbonyl)leucyl>glycinanilide 
• 127663-71-2 (N-(N-Benzyloxycarbonyl-leucyl)-glycyl)-diazomethan 
• 59179-81-6 2-benzoyl-4-chloro-N^α-leucylglycinanilide 
• 16295-32-2 N-{N-[N-(N-benzyloxycarbonyl-L-leucyl)-glycyl]-glycyl}-glycine 
• 14297-22-4 N-[N-(N-benzyloxycarbonyl-L-leucyl)-glycyl]-glycine 
• 92399-26-3 Z-Leu-Gly-Gln-N₂H₃*TFA 
• 92398-89-5 Z-Leu-Gly-Gln-N₂H₂-Boc 
• 4801-79-0 N-benzyloxycarbonyl-L-leucinamide 

Relevant articles and documents

SYNTHESIS OF SERINE PEPTIDES. I.

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