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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)-

2,4-Pyrimidinediamine, 6-chloro-N4-methyl-

CNc1cc(Cl)nc(n1)N Request for Quotation
Chemical Name: 2,4-Pyrimidinediamine, 6-chloro-N4-methyl-
CAS Number: 1005-37-4
Product Number: AG00025O(AGN-PC-0JOC3H)
Synonyms:
MDL No:
Molecular Formula: C5H7ClN4
Molecular Weight: 158.5889

Identification/Properties

Computed Properties
Molecular Weight:
158.589g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
158.036g/mol
Monoisotopic Mass:
158.036g/mol
Topological Polar Surface Area:
63.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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-H317-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-N4-methylpyrimidine-2,4-diamine, also known as $name$, serves as a valuable building block in chemical synthesis processes. This compound is commonly utilized in the pharmaceutical industry for the production of various drugs and bioactive molecules. Its unique chemical structure enables it to participate in a wide range of reactions, making it a versatile intermediate in organic synthesis. $name$ can be used as a precursor for the synthesis of key pharmaceutical compounds, such as antiviral or anticancer drugs, by undergoing functional group transformations or cyclization reactions. Additionally, its reactivity and compatibility with common reaction conditions make it a convenient reagent for the preparation of diverse chemical derivatives with tailored properties. Overall, the application of 6-Chloro-N4-methylpyrimidine-2,4-diamine in chemical synthesis provides chemists with a powerful tool for the efficient and strategic construction of complex molecules with potential biological activities.