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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)-

[1,2,4]Triazolo[1,5-a]pyrimidin-7-ol, 5-methyl-

Cc1cc(O)n2c(n1)ncn2 Request for Quotation
Chemical Name: [1,2,4]Triazolo[1,5-a]pyrimidin-7-ol, 5-methyl-
CAS Number: 2503-56-2
Product Number: AG003MUL(AGN-PC-0O88UZ)
Synonyms:
MDL No:
Molecular Formula: C6H6N4O
Molecular Weight: 150.1380

Identification/Properties

Properties
MP:
280-283 °C(lit.)
BP:
271.66°C (rough estimate)
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.6700 (estimate)
Computed Properties
Molecular Weight:
150.141g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
150.054g/mol
Monoisotopic Mass:
150.054g/mol
Topological Polar Surface Area:
57.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
302
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:
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


7-Hydroxy-5-methyl-1,3,4-triazaindolizine is a versatile compound frequently utilized in chemical synthesis for its unique reactivity and structural properties. In organic chemistry, this compound serves as a valuable building block for the synthesis of various bioactive molecules and pharmaceutical intermediates. Its specific chemical structure allows for the introduction of functional groups at different positions, enabling the production of diverse compounds with tailored properties. Additionally, 7-Hydroxy-5-methyl-1,3,4-triazaindolizine plays a crucial role in the development of new materials and catalysts, due to its ability to participate in various chemical reactions with high efficiency and selectivity. This compound's versatility and reactivity make it a valuable tool for researchers and chemists alike, contributing to advancements in both organic synthesis and materials science.