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768-93-4 | 1-Iodoadamantane
CAS No: 768-93-4 Catalog No: AG003EFP MDL No:
Product Description
Catalog Number:
AG003EFP
Chemical Name:
1-Iodoadamantane
CAS Number:
768-93-4
Molecular Formula:
C10H15I
Molecular Weight:
262.1306
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
InChI Key:
PXVOATXCSSPUEM-UHFFFAOYSA-N
SMILES:
IC12CC3CC(C2)CC(C1)C3
NSC Number:
169440
Properties
Complexity:
144
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
262.022g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
262.134g/mol
Monoisotopic Mass:
262.022g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.4
Literature
| Title | Journal |
|---|---|
| [1-(1-Adamantylamino)ethyl-idene]oxonium methane-sulfonate. | Acta crystallographica. Section E, Structure reports online 20090601 |
| Electrosynthetic reduction of 1-iodoadamantane forming 1,1'-biadamantane and adamantane in aprotic solvents: insonation switches the mechanism from dimerisation to exclusive monomer formation. | Ultrasonics sonochemistry 20070701 |
| 'One-step' alkynylation of adamantyl iodide with silver(I) acetylides. | Organic letters 20050331 |
| Radical-mediated carboxylation of alkyl iodides with [11C]carbon monoxide in solvent mixtures. | The Journal of organic chemistry 20050318 |
| Fluorescent quenching of the 2-naphthoxide anion by aliphatic and aromatic halides. Mechanism and consequences of electron transfer reactions. | The Journal of organic chemistry 20030321 |
| Regiochemistry of the photostimulated reaction of the phthalimide anion with 1-iodoadamantane and tert-butylmercury chloride by the S(RN)1 mechanism. | The Journal of organic chemistry 20020208 |
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