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Glutarimid

Glutarimide Struktur
1121-89-7
CAS-Nr.
1121-89-7
Bezeichnung:
Glutarimid
Englisch Name:
Glutarimide
Synonyma:
PIPERIDINE-2,6-DIONE;NSC 58190;NSC 168666;GLUTARIMIDE;Glutarimide98%;Glutarimide>2,6-Dioxopiperidine;2,6-PIPERIDINEDIONE;2,6-DIKETOPIPERIDINE;GlutariMide, 98% 25GR
CBNumber:
CB2221090
Summenformel:
C5H7NO2
Molgewicht:
113.11
MOL-Datei:
1121-89-7.mol

Glutarimid Eigenschaften

Schmelzpunkt:
155-157 °C (lit.)
Siedepunkt:
211.82°C (rough estimate)
Dichte
1.2416 (rough estimate)
Brechungsindex
1.4200 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
L?slichkeit
soluble in Chloroform, DCM
Aggregatzustand
Crystals or Crystalline Flakes
pka
pKa 11.4 (Uncertain)
Farbe
White
Wasserl?slichkeit
Soluble in water, hot ethanol and boiling benzene. Insoluble in ether.
BRN 
110052
InChI
InChI=1S/C5H7NO2/c7-4-2-1-3-5(8)6-4/h1-3H2,(H,6,7,8)
InChIKey
KNCYXPMJDCCGSJ-UHFFFAOYSA-N
SMILES
N1C(=O)CCCC1=O
CAS Datenbank
1121-89-7(CAS DataBase Reference)
EPA chemische Informationen
Glutarimide (1121-89-7)

Sicherheit

Kennzeichnung gef?hrlicher Xi
R-S?tze: 36
S-S?tze: 37/39-26
WGK Germany  3
RTECS-Nr. MA4000000
HS Code  29251995

Glutarimid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R36:Reizt die Augen.

S-S?tze Betriebsanweisung:

S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Chemische Eigenschaften

white crystalline powder

Verwenden

Glutarimide acts as an inhibitor of protein synthesis. Further, it is used as a reactant for thionations and biocatalytic asymmetric synthesis of sitagliptin production. It is also employed in the generation of beta-adrenoceptor ligands, enantioselective synthesis of securinega alkaloids and alfa-fluoro-alfa amino amides. In addition to this, it is used in intramolecular amidocyclopropanation reactions.

synthetische

To a flask containing 70 gm (0.53 mole) of glutaric acid is added 150 ml (2.2 mole) of 28% aqueous ammonia. The mixture is set for distillation and heated for 7 hr as the temperature of the mixture rises from 90° to 180°C. The temperature is held at 170-180°C for \\ hr or until the evolution of ammonia ceases. The reaction mixture solidifies on cooling and the pro­duct is recrystallized from acetone to afford 37.4 gm (63%), m.p. 145-146°C.
t may be advantageous to preform the ammonium salt of dicarboxylic acids prior to the application of enough heat to form the imide. The preparation of succinimide is a case in point.
Preparation of Glutarimide

Definition

ChEBI: Glutarimide (Piperidine-2,6-dione) is a dicarboximide that is piperidine which is substituted by oxo groups at positions 2 and 6. It is a member of piperidones and a dicarboximide.

Allgemeine Beschreibung

A glutarimide antibiotic, 9-methylstreptimidone, shows antiviral, antitumor and antifungal activities.

l?uterung methode

Purify it by dissolving 75g in 200mL of H2O, boil for 30minutes with 2g of charcoal, filter, evaporate to dryness and recystallise the residue from 125mL of 95% EtOH to give 70g of white crystals, m 152-154o. It also crystallises from Me2CO (m 163-165o) or EtOH (m 153-154o). The N-bromo derivative (a brominating agent) crystallises from H2O with m 180-185o. [Paris et al. Org Synth Coll Vol IV 496 1963, Beilstein 21 H 382, 21 I 331, 21 II 307, 21 III/IV 4582.]

Glutarimid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Glutarimid Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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1121-89-7(Glutarimid)Verwandte Suche:


  • GLUTARIMIDE
  • 2,6-PIPERIDINEDIONE
  • 2,6-DIKETOPIPERIDINE
  • Glutarimide98%
  • 2,6-Dioxopiperidine
  • GlutariMide, 98% 25GR
  • 2,6-Diketopiperidine 2,6-Piperidinedione
  • AcetylglycinaMide IMpurity B
  • NSC 58190
  • NSC 168666
  • Acetylglycinamide Impurity 2
  • Glutarimide>
  • PIPERIDINE-2,6-DIONE
  • 1121-89-7
  • Heterocyclic Building Blocks
  • Piperidines
  • Building Blocks
  • Building Blocks
  • Heterocyclic Building Blocks
  • Piperidines
  • Miscellaneous Biochemicals
  • organic intermediate
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