1-Iodoadamantane

HCID 136609CAS 768-93-4

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Basic information

Standard SMILES
IC12CC3CC(CC(C3)C1)C2
InChIKey
PXVOATXCSSPUEM-UHFFFAOYSA-N
Molecular formula
C10H15I
Average molar mass
262.134 g/mol
Monoisotopic mass
262.02184848

Names & identifiers

Preferred name
1-Iodoadamantane
IUPAC
1-Iodoadamantane
English name
1-Iodoadamantane
Molecular formula
C10H15I
Molecular weight
262.13

Names & synonyms

(3s,5s,7s)-1-iodoadamantaneNSC 1694401-IODOADAMANTANEAdamantyl iodide1-Adamantyl iodideRARECHEM AQ TC 1020Adamantane, 1-iodo-IFLAB-BB F0701-00781-Iodoadamantane 98%Adamantyl iodide,98%

Database identifiers

CAS
768-93-4
PubChem CID
136609
DTXSID
DTXSID00227619
Nikkaji
J329.828K

Properties

Physicochemical properties

Melting point
75 · 75-76 °C(lit.)
Boiling point
265.7 · 265.7±9.0℃ (760 Torr)
Density
1.63 · 1.63±0.1 g/cm3 (20 ºC 760 Torr)
refractive index
1.661 · 1.6610 (estimate)
Flash point
115.9 · 115.9±13.1℃
storage temp.
2 · 2-8°C(protect from light)

Safety & regulation

Safety data

PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
Storage Class
11 - Combustible Solids

Chemistry & industry

Applications · 2 items

Uses1-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.

General Description1-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.

Suppliers50 total

上海康恩博医药科技有限公司17510465506 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
郑州阿尔法化工有限公司+86-18530059196 · [email protected]
湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
湖北万得化工有限公司15377098680 15377098680 · [email protected]

Related reactions

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