1H-Pyrazole, 5-chloro-3-methyl-1-phenyl-


Chemical Name: 1H-Pyrazole, 5-chloro-3-methyl-1-phenyl-
CAS Number: 1131-17-5
Product Number: AG003MO0(AGN-PC-0KK7C4)
Synonyms:
MDL No:
Molecular Formula: C10H9ClN2
Molecular Weight: 192.6449

Identification/Properties


Properties
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
192.646g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
192.045g/mol
Monoisotopic Mass:
192.045g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
168
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-Chloro-3-methyl-1-phenyl-1H-pyrazole, also known as $name$, is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. In organic synthesis, this compound serves as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials.Its structural features make it an essential component in the development of novel molecules with biological activity. $name$ acts as a valuable intermediate in the synthesis of complex organic compounds, allowing chemists to introduce specific functional groups and tailor molecular structures for desired properties.Furthermore, the presence of the chloro and methyl substituents on the pyrazole ring of $name$ makes it a valuable starting material for diverse modifications, enabling the creation of structurally diverse compounds with potentially enhanced characteristics. Its application in chemical synthesis extends to the creation of advanced materials and the investigation of structure-activity relationships in drug discovery.Through strategic manipulation of its structure, $name$ can be transformed into a wide range of derivatives with varied chemical and biological functions, making it a valuable tool in the hands of synthetic chemists looking to explore new frontiers in drug development, material science, and beyond.