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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, 3,5-dimethyl-4-nitro-

[O-][N+](=O)c1c(C)n[nH]c1C Request for Quotation
Chemical Name: 1H-Pyrazole, 3,5-dimethyl-4-nitro-
CAS Number: 14531-55-6
Product Number: AG001KSI(AGN-PC-0JMUYP)
Synonyms:
MDL No:
Molecular Formula: C5H7N3O2
Molecular Weight: 141.1280

Identification/Properties

Properties
MP:
125.0 to 129.0 °C
BP:
304.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
141.13g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
141.054g/mol
Monoisotopic Mass:
141.054g/mol
Topological Polar Surface Area:
74.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
144
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chemical compound 3,5-Dimethyl-4-nitro-1H-pyrazole plays a crucial role in chemical synthesis as a versatile building block. With its unique structure, this compound serves as a key intermediate in the synthesis of various organic compounds. Its presence allows for the introduction of specific functional groups or substituents at precise positions, making it a valuable tool in the production of pharmaceuticals, agrochemicals, and specialty chemicals. In addition, 3,5-Dimethyl-4-nitro-1H-pyrazole can be utilized in the creation of heterocyclic compounds, providing access to diverse molecular frameworks for further exploration in drug discovery and materials science. Its compatibility with a range of synthetic methodologies makes it a valuable asset in the hands of chemists seeking to design and develop innovative chemical entities with tailored properties and functionalities.