105172-44-9

Basic information

• Product Name: [{9-[(carboxymethyl)amino]-3-ethyl-9-oxononanoyl}(ethyl)amino]acetic acid (non-preferred name)
• CAS NO: 105172-44-9
• Molecular Formula: C₁₇H₃₀N₂O₆
• Molecular Weight: 358.4299
• Mol File: 105172-44-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 633.2°C at 760 mmHg
• Flash Point: 336.7°C
• Density: 1.159g/cm³
• Vapor Pressure: 1.17E-17mmHg at 25°C
• Refractive Index: 1.502
• CAS DataBase Reference: [{9-[(carboxymethyl)amino]-3-ethyl-9-oxononanoyl}(ethyl)amino]acetic acid (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: [{9-[(carboxymethyl)amino]-3-ethyl-9-oxononanoyl}(ethyl)amino]acetic acid (non-preferred name)(105172-44-9)
• EPA Substance Registry System: [{9-[(carboxymethyl)amino]-3-ethyl-9-oxononanoyl}(ethyl)amino]acetic acid (non-preferred name)(105172-44-9)

Safety Data

• Hazardous Substances Data: 105172-44-9(Hazardous Substances Data)

Upstream product

• 123-99-9 azelaic acid 
• 123-98-8 azelaoyl chloride 
• 623-33-6 glycine ethyl ester hydrochloride 
• 105172-42-7 C₁₅H₂₄O₈ 

Relevant articles and documents

A METHOD OF SYNTHESISING AN AMINO ACID DERIVATIVE OF AZELAIC ACID

A method of producing an amide ester derivative of azelaic acid comprising treating an amino acid hydrohalide of the general formula (I): wherein R' is a substituted or unsubstituted alkyl, and R" is a substituted or unsubstituted side chain group of an amino acid selected from substituted or unsubstituted alkyl moiety, cyclic alkyl or aromatic moiety. The amino acid hydrohalide compound is to be dissolved in an aprotic solvent with an organic base to effect deprotonation, reacting the deprotonated product with an azelaic acid halide also dissolved in an aprotic solvent, contacting the reactant mixture with an anhydrous salt to remove any moisture therefrom and removing the aprotic solvent form the reactant mixture.

The synthesis and characterization of a series of bis-intercalating bis-anthracyclines

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