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7432-25-9

7432-25-9 Structure

7432-25-9 Structure
IdentificationBack Directory
[Name]

Etaqualone
[CAS]

7432-25-9
[Synonyms]

Aolan
Athinazone
Ethinazone
Etaqualone
Ethaqualone
Etaqualone (3-(2-Ethylphenyl)-2-met
2-Methyl-3-(o-ethylphenyl)-4-quinazolone
3-(2-ethylphenyl)-2-methylquinazolin-4-one
3-(2-Ethylphenyl)-2-methylquinazolin-4(3H)-one
3-(o-Ethylphenyl)-2-methyl-4(3H)-quinazolinone
2-Methyl-3-(2-ethylphenyl)-4(3H)-quinazolinone
4(3H)-Quinazolinone, 3-(2-ethylphenyl)-2-methyl-
Etaqualone, 3-(2-ethylphenyl)-2-Methyl-quinazolin-4-one
EtaqualoneQ: What is Etaqualone Q: What is the CAS Number of Etaqualone Q: What is the storage condition of Etaqualone Q: What are the applications of Etaqualone
[Molecular Formula]

C17H16N2O
[MOL File]

7432-25-9.mol
[Molecular Weight]

264.32
Chemical PropertiesBack Directory
[Melting point ]

81℃
[Boiling point ]

421.1±38.0 °C(Predicted)
[density ]

1.14
[solubility ]

DMF: 5 mg/ml; DMSO: 5 mg/ml; Ethanol: 12 mg/ml; Ethanol:PBS(pH 7.2) (1:1): 0.5 mg/ml
[form ]

A crystalline solid
[pka]

2.95±0.70(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Description]

Etaqualone (Item No. 11152) is an analytical reference standard categorized as a quinazolone. This product is intended for research and forensic applications.
[Uses]

Etaqualone is an analog of the hypnotic methaqualone, a non-barbiturate sedative also known as Quaalude. Methaqualone is regulated (Schedule I) in the United States. The physiological and toxicological properties of etaqualone have been poorly delineated. This product is intended for forensic and research applications.[Cayman Chemical]
[Uses]

Etaqualone is marketed as a sedative, hypnotic, muscle relaxant and central nervous system depressant. It has to ability to bind to the beta GABAA receptor which helps negate insomnia.
[Definition]

ChEBI:Etaqualone is a member of quinazolines.
[References]

[1] SURENDRA S. PARMAR. Role of alkyl substitution in 2,3-disubstituted and 3-substituted 4-quinazolones on the inhibition of pyruvic acid oxidation[J]. Journal of Medicinal Chemistry, 1969, 12 1: 138-141. DOI: 10.1021/jm00301a035
Tags:7432-25-9 Related Product Information

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