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1-Iodoadamantane

1-Iodoadamantane Struktur
768-93-4
CAS-Nr.
768-93-4
Englisch Name:
1-Iodoadamantane
Synonyma:
NSC 169440;1-IODOADAMANTANE;Adamantyl iodide;1-Adamantyl iodide;RARECHEM AQ TC 1020;Adamantane, 1-iodo-;IFLAB-BB F0701-0078;1-Iodoadamantane 98%;(3s,5s,7s)-1-iodoadamantane;Andrographolide sodium bisulfite
CBNumber:
CB2191577
Summenformel:
C10H15I
Molgewicht:
262.13
MOL-Datei:
768-93-4.mol

1-Iodoadamantane Eigenschaften

Schmelzpunkt:
75-76 °C(lit.)
Siedepunkt:
265.7±9.0℃ (760 Torr)
Dichte
1.63±0.1 g/cm3 (20 ºC 760 Torr)
Brechungsindex
1.6610 (estimate)
Flammpunkt:
115.9±13.1℃
storage temp. 
2-8°C(protect from light)
L?slichkeit
DMSO: 52 mg/mL (198.37 mM);;
Stabilit?t:
Stable, but light and moisture sensitive. Incompatible with strong oxidizing agents.
InChI
InChI=1S/C10H15I/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2
InChIKey
PXVOATXCSSPUEM-UHFFFAOYSA-N
SMILES
C12(I)CC3CC(CC(C3)C1)C2

Sicherheit

WGK Germany  3

1-Iodoadamantane Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

solid

Verwenden

1-Iodoadamantane is suitable reagent used to evaluate the rate constants for the reduction of haloadamantanes by SmI2 in presence of hexamethylphosphoramide (HMPA) and H2O by GC/MS-analyzed method. It may be used as iodine atom donor for probing the intermediacy of radical to investigate the chemistry of highly reactive, strained systems such as propellane. It may be used as starting reagent in the synthesis of N-(1-adamantyl)acetamide via nucleophilic substitution. It may be employed in the free-radical carbonylation reactions with alkenes.

Allgemeine Beschreibung

1-Iodoadamantane is a haloadamantane. Voltammetric reduction of 1-iodoadamantane at a silver cathode in tetrahydrofuran (THF) and acetonitrile (ACN) is reported to involve a single electron forming a mixture of monomeric and dimeric products. The photoinduced reaction of 1-iodoadamantane in DMSO is reported to afford substitution products on C3, C6, and C8, 1-adamantanol, 1-adamantyl 2-naphthyl ether, and adamantine. The photostimulated reaction of the phthalimide anion with 1-iodoadamantane is reported to yield 3-(1-adamantyl) phthalimide and 4-(1-adamantyl) phthalimide, along with the reduction product adamantane. 1-Iodoadamantane is reported to undergoe photostimulated reaction with the enolate anion of acetone, acetophenone and propiophenone to give admantane and the substitution products.

l?uterung methode

Dissolve the iodide in Et2O, shake with aqueous NaHSO3, aqueous K2CO3, and H2O, dry (Na2SO4), evaporate and recrystallise it from MeOH at -70o (to avoid alcoholysis) to give white crystals. [Schleyer & Nicholas J Am Chem Soc 83 2700 1961, lit m of 151-152.5o is incorrect.] Also purify by recrystallisation from pet ether (40-60oC) followed by rigorous drying and repeated sublimation. [Beilstein 5 IV 470.]

1-Iodoadamantane Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


1-Iodoadamantane Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 79)Lieferanten
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Capot Chemical Co.,Ltd.
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1026@dideu.com China 8670 58

768-93-4()Verwandte Suche:


  • IFLAB-BB F0701-0078
  • 1-IODOADAMANTANE
  • 1-Adamantyl iodide
  • Adamantane, 1-iodo-
  • RARECHEM AQ TC 1020
  • Adamantyl iodide
  • Tricyclo(3.3.1.13,7)decane, 1-iodo-
  • Tricyclo[3.3.1.13,7]decane, 1-iodo-
  • Andrographolide sodium bisulfite
  • NSC 169440
  • 1-Iodoadamantane 98%
  • (3s,5s,7s)-1-iodoadamantane
  • 1IODOADAMANTANE,1 IODOADAMANTANE
  • 768-93-4
  • C10H15I
  • C20H30O5NaHSO3
  • Building Blocks
  • Alkyl
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Alkyl
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Adamantane derivatives
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