1H-Benzimidazole, 4-chloro-2-methyl-


Chemical Name: 1H-Benzimidazole, 4-chloro-2-methyl-
CAS Number: 5599-82-6
Product Number: AG003L3O(AGN-PC-0K5W5K)
Synonyms:
MDL No:
Molecular Formula: C8H7ClN2
Molecular Weight: 166.6076

Identification/Properties


Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
166.608g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
166.03g/mol
Monoisotopic Mass:
166.03g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Chloro-2-methyl-1H-benzo[d]imidazole is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic synthesis, it serves as a valuable building block for the preparation of various biologically active compounds, pharmaceuticals, and agrochemicals. This heterocyclic compound is particularly sought after for its ability to participate in diverse chemical reactions, including nucleophilic substitution, cyclization, and metal-catalyzed transformations. Its presence in a molecule can impart specific biological activities or alter pharmacokinetic properties, making it a crucial intermediate in the synthesis of functional molecules. Additionally, 4-Chloro-2-methyl-1H-benzo[d]imidazole exhibits stability under a wide range of reaction conditions, making it an essential tool in the toolkit of synthetic chemists across different fields.