1. Home
  2. 4(3H)-Quinazolinone,8-bromo-6-methyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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,8-bromo-6-methyl-

Cc1cc(Br)c2c(c1)c(=O)[nH]cn2 Request for Quotation
Chemical Name: 4(3H)-Quinazolinone,8-bromo-6-methyl-
CAS Number: 215115-09-6
Product Number: AG00C3PX(AGN-PC-0QY1SX)
Synonyms:
MDL No:
Molecular Formula: C9H7BrN2O
Molecular Weight: 239.0687

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
239.072g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
237.974g/mol
Monoisotopic Mass:
237.974g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
254
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-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


8-Bromo-6-methylquinazolin-4(3H)-one is a versatile building block widely used in chemical synthesis for the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its unique molecular structure and reactive functional groups make it a valuable intermediate in the synthesis of biologically active compounds.This compound can serve as a key starting material in the synthesis of quinazoline derivatives, which exhibit diverse pharmacological activities such as anticancer, antimicrobial, and antiviral properties. By utilizing 8-Bromo-6-methylquinazolin-4(3H)-one as a core scaffold, chemists can efficiently access a range of structurally complex molecules through functional group transformations and strategic bond formations.Furthermore, 8-Bromo-6-methylquinazolin-4(3H)-one can be modified through substitution, cross-coupling reactions, and cyclization to introduce specific functionalities or improve the desired biological properties of the final products. Its versatility and synthetic potential make it a valuable tool in the hands of synthetic chemists for the rational design and creation of novel compounds with potential therapeutic applications.