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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Pyrazole, 3,4-dimethyl-

Cc1n[nH]cc1C Request for Quotation
Chemical Name: 1H-Pyrazole, 3,4-dimethyl-
CAS Number: 2820-37-3
Product Number: AG007L2R(AGN-PC-0O8K4N)
Synonyms:
MDL No:
Molecular Formula: C5H8N2
Molecular Weight: 96.1304

Identification/Properties

Computed Properties
Molecular Weight:
96.133g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
96.069g/mol
Monoisotopic Mass:
96.069g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
63.1
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#:
N/A
Hazard Statements:
H302-H319-H412
Precautionary Statements:
P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,4-Dimethyl-1H-pyrazole is a versatile chemical compound widely used in chemical synthesis processes. Its unique structure and properties make it a valuable building block for the creation of various organic compounds. 
One key application of 3,4-Dimethyl-1H-pyrazole is in the synthesis of pharmaceuticals. It serves as a key intermediate in the production of many medicinal compounds due to its ability to introduce specific functional groups and enhance the biological activity of the final drug products.
Furthermore, this compound is often utilized in the preparation of agrochemicals. By incorporating 3,4-Dimethyl-1H-pyrazole into the synthesis of pesticides and herbicides, researchers can fine-tune the properties and effectiveness of these agricultural chemicals for pest control and crop protection.
Additionally, 3,4-Dimethyl-1H-pyrazole finds applications in material science, particularly in the development of specialty polymers and advanced materials. Its presence in the polymerization process can impart specific characteristics such as thermal stability, mechanical strength, or desired optical properties to the final material.
In conclusion, the use of 3,4-Dimethyl-1H-pyrazole in chemical synthesis spans across various industries, showcasing its significance as a crucial component in the creation of diverse compounds with tailored properties and functionalities.