CAS 110349-26-3
:Benzoic acid, 2-iodo-, 1,1-dimethylethyl ester
Description:
Benzoic acid, 2-iodo-, 1,1-dimethylethyl ester, with the CAS number 110349-26-3, is an organic compound characterized by its ester functional group, which is formed from benzoic acid and an alcohol. This compound features a benzoic acid moiety substituted at the 2-position with an iodine atom, and it has a tert-butyl group (1,1-dimethylethyl) as part of its structure. The presence of the iodine atom can impart unique reactivity and properties, such as increased lipophilicity and potential for nucleophilic substitution reactions. Benzoic acid derivatives are often used in various applications, including as preservatives, flavoring agents, and in the synthesis of pharmaceuticals. The tert-butyl group contributes to the steric hindrance, which can influence the compound's reactivity and interactions with other molecules. Overall, this compound is of interest in organic synthesis and may exhibit specific biological activities due to its structural features.
Formula:C11H13IO2
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Found 4 products.
tert-Butyl 2-iodobenzoate
CAS:Formula:C11H13IO2Purity:98%Color and Shape:LiquidMolecular weight:304.1242t-Butyl 2-iodobenzoate
CAS:<p>t-Butyl 2-iodobenzoate is a reagent that can be used to access cyclopentenes. The reaction begins with the lithiation of an alkoxycarbonyl group and the subsequent attachment of an electrophilic cyclopentene. The reaction is completed by adding a tertiary amine, which causes carbopalladation of the alkyl lithium intermediate, forming a new carbon-carbon bond. Cyclopentenes can also be accessed by intramolecular reactions using a palladium catalyst and alkoxycarbonyl groups as substrates. Camptothecin moieties are often functionalized with t-butyl 2-iodobenzoate in order to access camptothecin analogs.</p>Formula:C11H13IO2Purity:Min. 95%Molecular weight:304.12 g/mol
