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64168-08-7

1-BENZYL-4-DIMETHYLAMINOPIPERIDINE

Catalog#: AR003EOQ  |   CAS#: 64168-08-7  |   MDL#: MFCD01084381  |   MF: C14H22N2  |   MW: 218.3379

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1g 98% $9.00 Global Stock Buy Now Add To Cart
5g 98% $30.00 Global Stock Buy Now Add To Cart
25g 98% $140.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003EOQ
Chemical Name 1-BENZYL-4-DIMETHYLAMINOPIPERIDINE
CAS Number 64168-08-7
Molecular Formula C14H22N2
Molecular Weight 218.3379
MDL Number MFCD01084381
SMILES CN(C1CCN(CC1)Cc1ccccc1)C

1-Benzyl-4-(dimethylamino)piperidine, commonly known as BDMAP, is a versatile compound widely used in chemical synthesis as a powerful nucleophilic reagent. Its unique structure and reactivity make it an indispensable tool in the preparation of various organic compounds.Due to the presence of a tertiary amine and a benzyl group in its structure, BDMAP exhibits strong nucleophilic properties, allowing it to participate in a wide range of transformations. One of the key applications of BDMAP is in the formation of carbon-carbon bonds through nucleophilic substitution reactions. By reacting with electrophilic substrates, BDMAP can facilitate the introduction of the dimethylamino-piperidine moiety into complex molecules, enabling the synthesis of novel compounds with diverse functionalities.Moreover, BDMAP can also serve as a useful reagent in the preparation of heterocyclic compounds. Its ability to undergo ring-closure reactions with suitable substrates makes it a valuable building block for the synthesis of various cyclic structures, including piperidine derivatives and other nitrogen-containing heterocycles.In addition to its role as a nucleophilic reagent, BDMAP can act as a chiral auxiliary in asymmetric synthesis. By incorporating BDMAP into the reaction pathway, chemists can control the stereochemistry of the final product, leading to the formation of enantiomerically enriched compounds with high optical purity.Overall, the application of 1-Benzyl-4-(dimethylamino)piperidine in chemical synthesis encompasses a wide range of reactions and transformations, making it a valuable reagent for organic chemists seeking to access new compounds and explore innovative synthetic strategies.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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