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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)-

Pyrazinamine, 3,5-dimethyl-

Cc1cnc(c(n1)C)N Request for Quotation
Chemical Name: Pyrazinamine, 3,5-dimethyl-
CAS Number: 91678-81-8
Product Number: AG006EGO(AGN-PC-0KKWE0)
Synonyms:
MDL No: MFCD00107172
Molecular Formula: C6H9N3
Molecular Weight: 123.1558

Identification/Properties

Properties
MP:
96 °C
BP:
243.457 °C at 760 mmHg
Storage:
Room Temperature;Light sensitive;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
123.159g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
123.08g/mol
Monoisotopic Mass:
123.08g/mol
Topological Polar Surface Area:
51.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
94.3
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-H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Dimethylpyrazin-2-amine is a versatile compound commonly used in chemical synthesis to introduce specific functional groups into molecules. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its reactivity and structural features. Its unique properties make it a key intermediate in the synthesis of a wide range of organic compounds, allowing chemists to tailor the structure and properties of target molecules for specific applications.