1H-Benzimidazole, 2-(chloromethyl)-1-(phenylmethyl)-


Chemical Name: 1H-Benzimidazole, 2-(chloromethyl)-1-(phenylmethyl)-
CAS Number: 7192-00-9
Product Number: AG005EX4(AGN-PC-0JSY6P)
Synonyms:
MDL No:
Molecular Formula: C15H13ClN2
Molecular Weight: 256.7301

Identification/Properties


Computed Properties
Molecular Weight:
256.733g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
256.077g/mol
Monoisotopic Mass:
256.077g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
265
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



1-Benzyl-2-(chloromethyl)-1H-benzo[d]imidazole is a versatile compound that finds wide application in chemical synthesis processes. Its strategic molecular structure combines a benzyl group, a chloromethyl group, and a benzo[d]imidazole core, allowing it to participate in a variety of chemical reactions to generate diverse functionalized molecules. In organic synthesis, this compound serves as a valuable building block for the construction of complex organic molecules due to its reactivity and the ability to introduce specific functionalities at desired positions. One of the key applications of 1-Benzyl-2-(chloromethyl)-1H-benzo[d]imidazole in chemical synthesis is in the synthesis of pharmaceutical intermediates. By utilizing the chloromethyl group as a versatile handle for further functionalization, chemists can selectively introduce various functional groups onto the benzo[d]imidazole core to produce novel drug candidates or key intermediates for pharmaceutical synthesis. Moreover, the benzyl group provides stability and protection to the reactive chloromethyl functionality, enabling precise control over the chemical transformations.Additionally, this compound plays a crucial role in the development of new materials and agrochemicals. The presence of the benzo[d]imidazole scaffold imparts unique properties to the synthesized materials, making them suitable for a range of applications such as optoelectronics, sensors, and crop protection chemicals. By incorporating 1-Benzyl-2-(chloromethyl)-1H-benzo[d]imidazole into the molecular design, chemists can access a diverse array of functional materials with tailored properties.Overall, the application of 1-Benzyl-2-(chloromethyl)-1H-benzo[d]imidazole in chemical synthesis is indispensable for the efficient construction of complex molecules with specific functionalities, making it a valuable tool for researchers across various scientific disciplines.