Lot numbers can be found on the outside label of a product:
1-Iodoadamantane
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CAS No. 768-93-4
- Cat. No. CS-0099591
- Purity≥97%
- MDL No.MFCD00134444
*For research and further manufacturing use only, not for direct human use.
Structure of 768-93-4
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General Information
- CAS No. 768-93-4
- Cat. No. CS-0099591
- Purity ≥97%
- MDL No. MFCD00134444
- Storage Sealed in dry,2-8℃
- Shipping Room temperature in continental US; may vary elsewhere.
- Molecular Formula C₁₀H₁₅I
- Molecular Weight 262.13
- Synonym(s) None
- SMILES IC1(C2)CC3CC2CC(C3)C1
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 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.
Synthesis
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Route1
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768-92-3 - ~98%
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In-stock
768-93-4
References
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Olah, George A.; Narang, Subhash C.; Field, Leslie D. Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3727 - 3728
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Route2
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In-stock
768-95-6 - ~10%
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In-stock
768-93-4
References
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Dobmeier, Michael; Herrmann, Josef M.; Lenoir, Dieter; Koenig, Burkhard Beilstein Journal of Organic Chemistry, 2012 , vol. 8, p. 330 - 336
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Route3
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In-stock
935-56-8 - ~94%
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In-stock
768-93-4
References
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Olah, George A.; Narang, Subhash C.; Field, Leslie D. Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3727 - 3728
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Safety Information
Download SDS|
GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Quality Control
Computational Chemistry Data
- TPSA 0
- LogP 3.3902
- H_Acceptors 0
- H_Donors 0
- Rotatable_Bonds 0
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Key Words
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