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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)-

4(3H)-Quinazolinone, 3-amino-2-methyl-

Nn1c(C)nc2c(c1=O)cccc2 Request for Quotation
Chemical Name: 4(3H)-Quinazolinone, 3-amino-2-methyl-
CAS Number: 1898-06-2
Product Number: AG002DZE(AGN-PC-0JODJE)
Synonyms:
MDL No:
Molecular Formula: C9H9N3O
Molecular Weight: 175.1873

Identification/Properties

Properties
MP:
149-152 °C(lit.)
BP:
348.1 °C at 760 mmH
Storage:
2-8℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
175.191g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
175.075g/mol
Monoisotopic Mass:
175.075g/mol
Topological Polar Surface Area:
58.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
262
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-2-methylquinazolin-4(3H)-one, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound is commonly used as a key intermediate in the preparation of various bioactive molecules and pharmaceuticals. Its functional groups and molecular scaffold make it a valuable starting material for the synthesis of diverse organic compounds.In chemical synthesis, 3-Amino-2-methylquinazolin-4(3H)-one can undergo a variety of reactions to introduce different functional groups and modify its structure. For example, the amino group can be selectively modified to introduce various substituents, allowing for the synthesis of derivatives with tailored properties. Additionally, the quinazolinone ring system provides a rigid framework for molecular design, making it particularly useful in the development of new drug candidates.Furthermore, 3-Amino-2-methylquinazolin-4(3H)-one can participate in condensation reactions with different reagents to form heterocyclic compounds or fused ring systems. This diversity in synthetic pathways enables the synthesis of complex molecules with specific biological activities or pharmacological profiles.Overall, the application of 3-Amino-2-methylquinazolin-4(3H)-one in chemical synthesis showcases its utility in organic chemistry and drug discovery, highlighting its importance as a valuable building block for the preparation of biologically active compounds and pharmaceutical agents.