CAS 7471-65-0
:1,2-Dimethyl-4(1H)-quinazolinone
Description:
1,2-Dimethyl-4(1H)-quinazolinone, with the CAS number 7471-65-0, is a heterocyclic organic compound characterized by a quinazolinone core structure. This compound features a fused bicyclic system that includes a benzene ring and a pyrimidine ring, with two methyl groups attached at the 1 and 2 positions of the quinazolinone moiety. It is typically a crystalline solid, exhibiting moderate solubility in organic solvents such as ethanol and dimethyl sulfoxide, while being less soluble in water. The compound is of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and anti-inflammatory properties. Its structure allows for various chemical modifications, which can enhance its pharmacological profile. Additionally, 1,2-Dimethyl-4(1H)-quinazolinone can serve as a building block in the synthesis of more complex molecules in drug development. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C10H10N2O
InChI:InChI=1/C10H10N2O/c1-7-11-10(13)8-5-3-4-6-9(8)12(7)2/h3-6H,1-2H3
InChI key:InChIKey=LKKQHIJMWGQCSO-UHFFFAOYSA-N
SMILES:CN1C=2C(C(=O)N=C1C)=CC=CC2
Synonyms:- 1,2-Dimethyl-4(1H)-quinazolone
- 1,2-Dimethylquinazolin-4(1H)-one
- Glomerine
- 4(1H)-Quinazolinone, 1,2-dimethyl-
- 1,2-Dimethyl-4(1H)-quinazolinone
- 4(1H)-quinazolinone, 1,2-dimethyl-
- Glomerin
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Found 2 products.
1,2-Dimethylquinazolin-4(1H)-one
CAS:Controlled Product1,2-Dimethylquinazolin-4(1H)-one is a chloride compound that reacts with methyl anthranilate to form the corresponding quinazolinones. The quinazolinones are a type of dicarbonyl and an anti-tumor agent that can be used in the treatment of cancer. 1,2-Dimethylquinazolin-4(1H)-one has been shown to inhibit the growth of certain cancer cells by inhibiting the synthesis of nucleic acid molecules and dicarbonyl. It also inhibits DNA replication and protein synthesis. 1,2-Dimethylquinazolin-4(1H)-one has been shown to interfere with the function of chloride channels in animal cells by binding to the chloride ion receptor site on the channel protein. This results in a slow reaction rate and an increase in immobilization.Formula:C10H10N2OPurity:Min. 95%Molecular weight:174.2 g/mol

