2(1H)-Quinolinone,7-hydroxy-4-methyl- structure
|
Common Name | 2(1H)-Quinolinone,7-hydroxy-4-methyl- | ||
---|---|---|---|---|
CAS Number | 20513-71-7 | Molecular Weight | 175.18400 | |
Density | 1.264 g/cm3 | Boiling Point | 417.8ºC at 760 mmHg | |
Molecular Formula | C10H9NO2 | Melting Point | ≥250ºC(lit.) | |
MSDS | Chinese USA | Flash Point | 206.5ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of 2(1H)-Quinolinone,7-hydroxy-4-methyl-7-Hydroxy-4-methyl-2(1H)-quinolone (compound 2b) is a fluorescent hydroxylated product. 7-Hydroxy-4-methyl-2(1H)-quinolone can be used for detecting hydroxyl radicals of DNA damage[1]. |
Name | 7-Hydroxy-4-methyl-2(1H)-quinolone |
---|---|
Synonym | More Synonyms |
Description | 7-Hydroxy-4-methyl-2(1H)-quinolone (compound 2b) is a fluorescent hydroxylated product. 7-Hydroxy-4-methyl-2(1H)-quinolone can be used for detecting hydroxyl radicals of DNA damage[1]. |
---|---|
Related Catalog | |
References |
Density | 1.264 g/cm3 |
---|---|
Boiling Point | 417.8ºC at 760 mmHg |
Melting Point | ≥250ºC(lit.) |
Molecular Formula | C10H9NO2 |
Molecular Weight | 175.18400 |
Flash Point | 206.5ºC |
Exact Mass | 175.06300 |
PSA | 53.09000 |
LogP | 1.54210 |
Vapour Pressure | 1.42E-07mmHg at 25°C |
Index of Refraction | 1.611 |
Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi |
Risk Phrases | R36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
HS Code | 2933790090 |
Precursor 8 | |
---|---|
DownStream 1 | |
HS Code | 2933790090 |
---|---|
Summary | 2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0% |
On the metabolism of quinoline and isoquinoline: possible molecular basis for differences in biological activities.
Carcinogenesis 4 , 1169-1173, (1983) Quinoline is a hepatocarcinogen in mice and rats, a mutagen in Salmonella typhimurium, and induces unscheduled DNA synthesis in primary cultures of rat hepatocytes. In contrast, isoquinoline has not b... |
|
Microbial metabolism of quinoline and related compounds. XIX. Degradation of 4-methylquinoline and quinoline by Pseudomonas putida K1.
Biol. Chem. Hoppe-Seyler 374 , 479-488, (1993) A bacterial strain, designated K1, which utilizes 4-methylquinoline and quinoline as sole source of carbon, nitrogen and energy was isolated from soil. Based on its morphological and physiological cha... |
7-hydroxy-4-methyl-1H-quinolin-2-one |
2,7-Dihydroxy-4-methylquinoline 7-Hydroxy-4-methylcarbostyryl |