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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-4,5-diamine, 1-methyl-, sulfate

OS(=O)(=O)O.Nc1c(N)cnn1C Request for Quotation
Chemical Name: 1H-Pyrazole-4,5-diamine, 1-methyl-, sulfate
CAS Number: 20055-01-0
Product Number: AG002CU6(AGN-PC-03HHHE)
Synonyms:
MDL No:
Molecular Formula: C4H10N4O4S
Molecular Weight: 210.2116

Identification/Properties

Computed Properties
Molecular Weight:
210.208g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
0
Exact Mass:
210.042g/mol
Monoisotopic Mass:
210.042g/mol
Topological Polar Surface Area:
153A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
165
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-1H-pyrazole-4,5-diamine sulfate is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceutical intermediates and specialty chemicals. In chemical synthesis, 1-Methyl-1H-pyrazole-4,5-diamine sulfate plays a crucial role as a nucleophilic reagent, facilitating the formation of complex molecular structures through selective substitution reactions. Its sulfated form enhances solubility and stability, making it an ideal choice for reactions requiring aqueous environments. By incorporating 1-Methyl-1H-pyrazole-4,5-diamine sulfate into synthesis pathways, chemists can efficiently access a diverse range of compounds with tailored properties and functionalities.