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ChemicalBook > Product Catalogue >Organic Chemistry >Hydrocarbons and derivatives >Hydrocarbon halides >1-Iodoadamantane

1-Iodoadamantane

1-Iodoadamantane Structure
  • ₹11370
  • Product name: 1-Iodoadamantane
  • CAS: 768-93-4
  • MF: C10H15I
  • MW: 262.13
  • EINECS:
  • MDL Number:MFCD00134444
  • Synonyms: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-
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Brand

  • Sigma-Aldrich
  • Sigma-Aldrich(India)

Package

  • 5G
  • ManufacturerSigma-Aldrich
  • Product number377198
  • Product description1-Iodoadamantane 98%
  • Packaging5G
  • Price₹11370
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number377198
  • Product description1-Iodoadamantane 98%
  • Packaging5G
  • Price₹11370
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich 377198 1-Iodoadamantane 98% 5G ₹11370 2022-06-14 Buy
Sigma-Aldrich(India) 377198 1-Iodoadamantane 98% 5G ₹11370 2022-06-14 Buy

Properties

Melting point :75-76 °C(lit.)
Boiling point :265.7±9.0℃ (760 Torr)
Density :1.63±0.1 g/cm3 (20 ºC 760 Torr)
refractive index :1.6610 (estimate)
Flash point :115.9±13.1℃
storage temp. :2-8°C(protect from light)
solubility :DMSO: 52 mg/mL (198.37 mM);;
Stability :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

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

1-Iodoadamantane is suitable reagent used to evaluate the rate constants for the reduction of haloadamantanes by SmI2in 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 ofN-(1-adamantyl)acetamidevianucleophilic substitution.It may be employed in the free-radical carbonylation reactions with alkenes.

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