GLYCINE ANHYDRIDE

GLYCINE ANHYDRIDE
  • CAS No.:106-57-0
Other grades of this product :
GLYCINE ANHYDRIDE Basic information
Product Name:GLYCINE ANHYDRIDE
Synonyms:PIPERAZINE-2,5-DIONE;Glycine EP Impurity B;Oxiracetam-1;2,5-Dioxopiperazin;2,5-Dioxopiperazine lactam;2,5-Piperazindion;alpha,gamma-Diacipiperazine;Cyclic(glycylglycyl)
CAS:106-57-0
MF:C4H6N2O2
MW:114.1
EINECS:203-411-5
Product Categories:
Mol File:106-57-0.mol
GLYCINE ANHYDRIDE Chemical Properties
Melting point >300 °C (lit.)
Boiling point 213.59°C (rough estimate)
density 1.3565 (rough estimate)
refractive index 1.4487 (estimate)
storage temp. Store below +30°C.
solubility 142g/l
pka12.88±0.20(Predicted)
form Crystalline Powder
color White to slightly yellow
Water Solubility Soluble in water (142mg/L).
Merck 14,7466
BRN 112112
InChIKeyBXRNXXXXHLBUKK-UHFFFAOYSA-N
CAS DataBase Reference106-57-0(CAS DataBase Reference)
EPA Substance Registry System2,5-Piperazinedione (106-57-0)
Safety Information
Safety Statements 24/25
WGK Germany 3
RTECS TL6325250
TSCA Yes
HS Code 29335990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
GLYCINE ANHYDRIDE Usage And Synthesis
Chemical Propertieswhite to slightly yellow crystalline powder
Uses2,5-Piperazinedione, can be used as an intermediate in the preparation of various pharmaceutical and biologically active compounds. It can be used in the synthesis of dipeptide isosteres by cross-metathesis.
DefinitionChEBI: A cyclic peptide that is piperazine in which the hydrogens at positions 2 and 5 are replaced by oxo groups.
Synthesis Reference(s)Journal of the American Chemical Society, 87, p. 4646, 1965 DOI: 10.1021/ja00948a047
Purification MethodsRecrystallise glycine anhydride from H2O (plates) and it can be sublimed (slowly) at 260o or at 140-170o/0.5mm. The dihydrochloride has m 129-130o and is prepared by dissolving it in conc HCl and adding EtOH to crystallisation point; dry it in a vacuum. The bis-1-naphthylurethane has m 232o(dec), and the diperchlorate has m 117o (hygroscopic). [MS: Johnstone J Chem Soc, Perkin Trans 1 1297 1975, NMR: Blaha & Samek Collect Czech Chem Commun 32 3780 1967, Sauborn J Phys Chem 36 179 1932, Corey J Am Chem Soc 60 1599 1938, Beilstein 24 IV 1070.]

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