159652-30-9

Basic information

• Product Name: BOC-D-DAP(BOC)-OH DCHA
• Synonyms: BOC-D-DAP(BOC)-OH DCHA;N-ALPHA,N-BETA-DI-BOC-D-2,3-DIAMINOPROPIONIC ACID DICYCLOHEXYLAMINE SALT;N2,N3-DI-BOC-D-2,3-DIAMINOPROPIONIC ACID DICYCLOHEXYLAMINE SALT;N-Boc-3-(Boc-amino)-D-alanine
• CAS NO: 159652-30-9
• Molecular Formula: C₁₃H₂₄N₂O₆
• Molecular Weight: 485.66
• Mol File: 159652-30-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 469.0±40.0 °C(Predicted)
• Appearance: /
• Density: 1.157±0.06 g/cm3(Predicted)
• PKA: 3.69±0.10(Predicted)
• CAS DataBase Reference: BOC-D-DAP(BOC)-OH DCHA(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-D-DAP(BOC)-OH DCHA(159652-30-9)
• EPA Substance Registry System: BOC-D-DAP(BOC)-OH DCHA(159652-30-9)

Safety Data

• Hazardous Substances Data: 159652-30-9(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 1482-97-9 (2R)-2,3-diaminopropanoic acid monohydrochloride 
• 259825-43-9 (R)-2-amino-3-((tert-butoxycarbonyl)amino)propanoic acid 
• 515-94-6 D-DAP 
• 73259-81-1 (R)-2-tert-butoxycarbonyl-3-aminopropionic acid 
• 7536-55-2 N-t-butyloxycarbonyl-D-asparagine 
• 541-16-2 t-butyl malonate 

Downstream Products

• 1429555-68-9 C₂₃H₄₂N₄O₅ 
• 1429555-43-0 C₂₃H₃₆N₄O₅ 
• 1426408-65-2 {(R)-2-tert-butoxycarbonylamino-2-[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-ylcarbamoyl]-ethyl}carbamic acid tert-butyl ester 

Relevant articles and documents

COMPOUNDS THAT TRAP ALPHA-OXOALDEHYDES AND ALPHA-BETA-UNSATURATED ALDEHYDES, META-COMPOUNDS CONTAINING SUCH COMPOUNDS, AND USE OF SAID COMPOUNDS IN TREATING ILLNESSES RELATED TO THE ACCUMULATION OF AGES AND ALES

The present invention relates to a series of molecules derived from 2,3-diaminopropionic acid (DAP), comprising or not comprising an 8-hydroxyquinoline (8-HQ) motif, and to the use of said molecules for trapping an alpha-oxoaldehyde resulting particularly from the degradation of the glucose or for trapping an alpha-beta-unsaturated aldehyde, resulting particularly from the oxidative degradation of fatty acids. These molecules can have a further application in the fields of cosmetics, food processing, and pharmaceuticals.

New 2,3-diaminopropionic acid inhibitors of AGE and ALE formation

Novel 2,3-diaminopropionic acid-based molecules were synthesised and tested successfully as glyoxal/methylglyoxal scavengers and as AGE inhibitors. Addition of an 8-hydroxyquinoline moiety led to an increase of the overall activity. The compounds tested in this study were also proved to be efficient in trapping ALE precursor malondialdehyde. The Royal Society of Chemistry 2013.