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1-Iodoadamantane - 95%, high purity , CAS No.768-93-4

    Grade & Purity:
  • ≥95%
In stock
Item Number
I472626
Grouped product items
SKU Size
Availability
Price Qty
I472626-1g
1g
5
$69.90
I472626-5g
5g
3
$259.90
View related series
Haloadamantane (1)

Basic Description

Synonyms 1-odoadamantane | (3s,5s,7s)-1-iodoadamantane | 1-Adamantyl iodide | Adamantyl iodide | 1-iodo-adamantane | 1-Iodotricyclo[3.3.1.13,7]decane
Specifications & Purity ≥95%
Storage Temp Store at 2-8°C,Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Description

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.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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organohalogen compounds
Class Organoiodides
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Organoiodides
Alternative Parents Hydrocarbon derivatives  Alkyl iodides  
Molecular Framework Aliphatic homopolycyclic compounds
Substituents Hydrocarbon derivative - Organoiodide - Alkyl iodide - Alkyl halide - Aliphatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as organoiodides. These are compounds containing a chemical bond between a carbon atom and an iodine atom.
External Descriptors Not available

Product Properties

ALogP 3.665

Names and Identifiers

Pubchem Sid 488187889
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488187889
IUPAC Name 1-iodoadamantane
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 C1C2CC3CC1CC(C2)(C3)I
Isomeric SMILES C1C2CC3CC1CC(C2)(C3)I
Molecular Weight 262.13
Reaxy-Rn 2038787
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2038787&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number Certificate Type Date Item
K2425407 Certificate of Analysis Nov 13, 2024 I472626
K2425416 Certificate of Analysis Nov 13, 2024 I472626
C2301720 Certificate of Analysis Feb 20, 2023 I472626
C2301712 Certificate of Analysis Feb 20, 2023 I472626

Chemical and Physical Properties

Sensitivity Moisture sensitive;Light sensitive
DMSO(mg / mL) Max Solubility 52
DMSO(mM) Max Solubility 198.374852172586
Water(mg / mL) Max Solubility -1
Melt Point(°C) 75-76 °C (lit.)
Molecular Weight 262.130 g/mol
XLogP3 4.400
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 0
Exact Mass 262.022 Da
Monoisotopic Mass 262.022 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 144.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

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