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939759-26-9

Benzyl 3-iodoazetidine-1-carboxylate

Catalog#: AR005XGI  |   CAS#: 939759-26-9  |   MDL#: MFCD09026510  |   MF: C11H12INO2  |   MW: 317.1230

Packsize Purity Price Availability Quantity
100mg 97% $9.00 Global Stock Buy Now Add To Cart
250mg 97% $11.00 Global Stock Buy Now Add To Cart
1g 97% $21.00 Global Stock Buy Now Add To Cart
5g 97% $75.00 Global Stock Buy Now Add To Cart
10g 97% $148.00 Global Stock Buy Now Add To Cart
25g 97% $347.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005XGI
Chemical Name Benzyl 3-iodoazetidine-1-carboxylate
CAS Number 939759-26-9
Molecular Formula C11H12INO2
Molecular Weight 317.1230
MDL Number MFCD09026510
SMILES IC1CN(C1)C(=O)OCc1ccccc1

Benzyl 3-iodoazetidine-1-carboxylate is a valuable compound widely utilized in chemical synthesis processes. This versatile reagent serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural features and reactivity.In chemical synthesis, Benzyl 3-iodoazetidine-1-carboxylate is frequently employed as a precursor in the preparation of heterocyclic compounds. Its iodine-containing functional group enables selective transformations through cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings, leading to the formation of complex molecular structures. This compound is particularly valuable for the introduction of the azetidine moiety into organic molecules, offering opportunities for the development of novel compounds with diverse biological activities.Additionally, Benzyl 3-iodoazetidine-1-carboxylate plays a crucial role in the synthesis of chiral compounds. Its azetidine ring provides a conformational restriction that aids in the control of stereochemistry during synthetic transformations, facilitating the creation of enantiomerically pure substances. This feature is essential in the pharmaceutical industry for the production of optically active drugs and chemical intermediates.Overall, Benzyl 3-iodoazetidine-1-carboxylate serves as a valuable tool in chemical synthesis, enabling the efficient construction of complex molecules with diverse functionalities and stereochemistries. Its applications extend across various sectors of the chemical industry, demonstrating its significance as a key reagent in modern synthetic processes.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P280-P301+P312-P302+P352-P305+P351+P338
Class N/A
Packing Group N/A

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