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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(1H)-Quinazolinone, 2-chloro-6-methyl-

Cc1ccc2c(c1)c(=O)nc([nH]2)Cl Request for Quotation
Chemical Name: 4(1H)-Quinazolinone, 2-chloro-6-methyl-
CAS Number: 62484-42-8
Product Number: AG00EKN1(AGN-PC-00NC0K)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2O
Molecular Weight: 194.61768

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-6-methylquinazolin-4(3H)-one is a versatile compound widely used in chemical synthesis for the preparation of various biologically active molecules. Its unique structure and reactivity make it a valuable building block in organic chemistry. This compound can undergo reactions such as nucleophilic substitution, Friedel-Crafts acylation, and cyclization to yield complex molecular structures. In pharmaceutical research, 2-Chloro-6-methylquinazolin-4(3H)-one is utilized for the synthesis of potential drug candidates due to its ability to introduce specific functional groups and stereochemical elements into the target molecules. Additionally, it serves as a key intermediate in the production of agrochemicals, specialty chemicals, and materials used in the field of medicinal chemistry. The diverse range of applications of 2-Chloro-6-methylquinazolin-4(3H)-one highlights its significance in the realm of chemical synthesis and underscores its importance in the creation of novel compounds with potential biological activities.