2130-77-0

Basic information

• Product Name: H-DAB(Z)-OH
• Synonyms: H-DAB(Z)-OH;(2S)-2-Amino-4-[[(phenylmethoxy)carbonyl]amino]butanoic acid;N4-(Benzyloxycarbonyl)-L-2,4-diaminobutanoic acid;L-Dab(Z)-OH;Nγ-Z-L-2,4-diaminobutyric acid≥ 97% (NMR);N-GAMMA-CARBOBENZOXY-L-2,4-DIAMINOBUTYRIC ACID
• CAS NO: 2130-77-0
• Molecular Formula: C₁₂H₁₆N₂O₄
• Molecular Weight: 252.27
• Mol File: 2130-77-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 225-227 °C
• Boiling Point: 483.2±45.0 °C(Predicted)
• Appearance: /
• Density: 1.266±0.06 g/cm3(Predicted)
• PKA: 2.25±0.10(Predicted)
• CAS DataBase Reference: H-DAB(Z)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-DAB(Z)-OH(2130-77-0)
• EPA Substance Registry System: H-DAB(Z)-OH(2130-77-0)

Safety Data

• Hazardous Substances Data: 2130-77-0(Hazardous Substances Data)

Usage

Chemical Properties

White solid

Upstream product

• 31139-36-3 dibenzyl dicarbonate 
• 305-62-4 L-2,4-diaminobutyric acid 
• 1758-80-1 L-2,4-diaminobutyrate 
• 501-53-1 benzyl chloroformate 
• 1482-98-0 L-2,4-diaminobutyric acid monohydrochloride 

Downstream Products

• 3350-20-7 (2S)-4-(benzyloxycarbonyl)amino-2-(tert-butoxycarbonyl)aminobutyric acid 
• 97868-86-5 N^α-palmitoyl-N^γ-benzyloxycarbonyl-L-α,γ-diaminobutyric acid 
• 5619-26-1 [2-((S)-2,5-dioxo-oxazolidin-4-yl)-ethyl]-carbamic acid benzyl ester 
• 802829-17-0 N(γ)-Benzyloxycarbonyl-L-α,γ-diamino-butyryl-L-threonin-methylester 
• 10403-31-3 N(γ)-Benzyloxycarbonyl-N(α)-(2-nitrophenylsulfenyl)-α,γ-diamino-butyryl-L-threonin-methylester 
• 55528-35-3 methyl (2S) 4-N-benzyloxycarbonyl-(2,4)-diaminobutyrate 
• 868740-32-3 L-α-<(L-α-Octanoylamino-γ-benzyloxycarbonylamino-butyryl)-amino>-γ-benzyloxycarbonylamino-buttersaeure 
• 868740-25-4 L-α-Octanoylamino-γ-benzyloxycarbonylamino-buttersaeure-methylester 
• 103097-59-2 N-[(S)-4-benzyloxycarbonylamino-2-(toluene-4-sulfonylamino)-butyryl]-glycine benzyl ester 

Relevant articles and documents

A new approach to the synthesis of selectively protected (2S)-1,2,4-triaminobutane derivatives

An efficient synthesis of selectively protected (2S)-1,2,4-triaminobutane from L-glutamic acid via (2S)-N4-benzyloxycarbonyl-2,4- diaminobutanamid is described. Georg Thieme Verlag Stuttgart.

Preparation and use of biotinylated ligands for LHRH receptor purification.

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