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AB44709

1182284-45-2 | 4-(Chloromethyl)-1-methylpiperidine hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $26.00 $18.00 -   +
250mg 95% in stock $35.00 $24.00 -   +
1g 95% in stock $44.00 $31.00 -   +
5g 95% in stock $149.00 $105.00 -   +
100g 95% in stock $2,002.00 $1,402.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB44709
Chemical Name: 4-(Chloromethyl)-1-methylpiperidine hydrochloride
CAS Number: 1182284-45-2
Molecular Formula: C7H15Cl2N
Molecular Weight: 184.1067
MDL Number: MFCD12923013
SMILES: ClCC1CCN(CC1)C.Cl

 

Computed Properties
Complexity: 77  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 4-(Chloromethyl)-1-methylpiperidine Hydrochloride is a versatile compound widely used in chemical synthesis as a key building block in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it particularly valuable in the production of complex organic molecules through a range of synthetic methodologies.The compound's chloromethyl group serves as a valuable handle for further functionalization, allowing for the introduction of diverse chemical moieties during the synthesis process. This feature enables chemists to tailor the compound to specific applications by modifying its structure in a controlled manner. Additionally, the presence of the piperidine ring provides opportunities for stereochemical control and molecular diversity, further enhancing the compound's utility in chemical synthesis.In the pharmaceutical industry, 4-(Chloromethyl)-1-methylpiperidine Hydrochloride is frequently employed in the development of novel drug candidates and intermediates. Its role in the synthesis of biologically active compounds highlights its significance as a key intermediate in medicinal chemistry research. Similarly, the compound finds application in the creation of specialized agrochemicals and fine chemicals, where its reactivity and versatility are essential for the construction of complex molecular architectures.Overall, the use of 4-(Chloromethyl)-1-methylpiperidine Hydrochloride in chemical synthesis exemplifies its importance as a strategic building block with broad applications across various sectors of the chemical industry.
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