
CAS Number491-36-1
SynonymsMFCD00511302; Quinazolone,4; 3,4-Dihydro-4-oxoquinazoline; QUINAZOLONE; T66 BVN EMJ; QUINAZOLIN-4-OL; 4-oxo-3,4-dihydroquinazoline; T66 BVM ENJ; 4-QUINAZOLINO; 4(3H)-Quinazolinone; 3,4-dihydroquinazolin-4-one; quinazolin-4(3H)-one; 3H-quinazolinyl-4-one; quinazoline-4(3H)-one; 4-QUINAZOLONE; 4-Quinazolinol; T66 BN DNJ EQ; EINECS 207-735-8; 4-Hydroxyquinazoline; Quinazolin-4-one; 4(1H)-Quinazolinone; QUINAZOLINONE; 4-HQN
Molecular FormulaC8H6N2O
Molecular Weight146.15
Purity98%
Density1.3±0.1 g/cm3
Boiling Point324.8±15.0 °C at 760 mmHg
Melting Point216-219 °C (lit.)
Appearancewhite solid
EINECS207-735-8
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 491-36-1 |
| Catalog No. | 2A-9022225 |
| Chinese Name | 4-Quinazolinone |
| Synonyms | MFCD00511302; Quinazolone,4; 3,4-Dihydro-4-oxoquinazoline; QUINAZOLONE; T66 BVN EMJ; QUINAZOLIN-4-OL; 4-oxo-3,4-dihydroquinazoline; T66 BVM ENJ; 4-QUINAZOLINO; 4(3H)-Quinazolinone; 3,4-dihydroquinazolin-4-one; quinazolin-4(3H)-one; 3H-quinazolinyl-4-one; quinazoline-4(3H)-one; 4-QUINAZOLONE; 4-Quinazolinol; T66 BN DNJ EQ; EINECS 207-735-8; 4-Hydroxyquinazoline; Quinazolin-4-one; 4(1H)-Quinazolinone; QUINAZOLINONE; 4-HQN |
| Molecular Formula | C8H6N2O |
| Molecular Weight | 146.15 |
| Purity | 98 |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 324.8±15.0 °C at 760 mmHg |
| Melting Point | 216-219 °C (lit.) |
| Appearance | white solid |
| Storage Condition | Use and store according to specifications, will no |
| Application | 4(3H)-Quinazolinone is a building block in chemical synthesis. Bioactive nitrogen heterocyclic compounds. It has a broad spectrum of biological properties, such as antibacterial, antifungal, anticonvu |
| EINECS | 207-735-8 |
| HTC | 29335995 |
| PubChem ID | 24895709 |
| MDL Number | MFCD00511302 |
| SMILES | O=C1NC=Nc2ccccc12 |
| InChI | 1S/C8H6N2O/c11-8-6-3-1-2-4-7(6)9-5-10-8/h1-5H,(H,9,10,11) |
| InChI Key | QMNUDYFKZYBWQX-UHFFFAOYSA-N |
| NACRES Code | NA.22 |
| UNSPSC | 12352100 |
| Hazard Symbols | Transport |
| MSDS | msds/22225_1_491_36_1.pdf |
| Bioactivity | 4(3H)-Quinazolinone is a building block in chemical synthesis. Biologically active nitrogen heterocyclic compounds. Possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anti-HIV, anticancerous and analgesic activities[1][2]. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Cancer Research Areas >> Endocrinology Research Areas >> Inflammation/Immunology Research Areas >> Infection Research Areas >> Metabolic Disease Research Areas >> Neurological Disease References [1]. Jafari E, et al. Quinazolinone and quinazoline derivatives: recent structures with potent antimicrobial and cytotoxic activities. Res Pharm Sci. 2016 Jan-Feb;11(1):1-14. [2]. Hameed A, et al. Quinazoline and quinazolinone as important medicinal scaffolds: a comparative patent review (2011-2016). Expert Opin Ther Pat. 2018 Apr;28(4):281-297. Chemical & Physical Properties Density 1.3±0.1 g/cm3 Boiling Point 324.8±15.0 °C at 760 mmHg Melting Point 216-219 °C(lit.) Molecular Formula C8H6N2O Molecular Weight 146.146 Flash Point 150.2±20.4 °C Exact Mass 146.048019 PSA 45.75000 LogP 0.30 Vapour Pressure 0.0±0.7 mmHg at 25°C Index of Refraction 1.705 InChIKey QMNUDYFKZYBWQX-UHFFFAOYSA-N SMILES O=c1[nH]cnc2ccccc12 Storage condition Desiccate at RT |
| Use of | 4(3H)-Quinazolinone is a building block in chemical synthesis. Biologically active nitrogen heterocyclic compounds. Possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anti-HIV, anticancerous and analgesic activities[1][2]. Properties Name 4-Hydroxyquinazoline Synonym More Synonyms 4-Quinazolinone Biological Activity Description 4(3H)-Quinazolinone is a building block in chemical synthesis. Biologically active nitrogen heterocyclic compounds. Possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anti-HIV, anticancerous and analgesic activities[1][2]. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Cancer Research Areas >> Endocrinology Research Areas >> Inflammation/Immunology Research Areas >> Infection Research Areas >> Metabolic Disease Research Areas >> Neurological Disease References [2]. Hameed A, et al. Quinazoline and quinazolinone as important medicinal scaffolds: a comparative patent review (2011-2016). Expert Opin Ther Pat. 2018 Apr;28(4):281-297. Chemical & Physical Properties Molecular Formula C8H6N2O Exact Mass 146.048019 PSA 45.75000 Index of Refraction 1.705 InChIKey QMNUDYFKZYBWQX-UHFFFAOYSA-N Storage condition Desiccate at RT |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available See reverse side of invoice or packing slip. |
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