Name | salicylanilide |
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Synonyms |
2-Phenylaminocarbonylphenol
Salinide Benzamide, 2-hydroxy-N-phenyl- Salicylanilid 2-Hydroxy-N-phenylbenzamide Salifebrin Ansadol salicylamide salicylic acid anilide N-Phenylsalicylamide Hyanilid EINECS 201-727-8 2-hydroxy-N-phenyl-benzamide Aseptolan Salicylanilide MFCD00002212 |
Description | Salicylanilide demonstrates a wide range of biological activities including antiviral potency which can inhibit HIV virus by targeting HIV-1 integrase or reverse transcriptase. |
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Related Catalog | |
Target |
HIV-1 integrase, reverse transcriptase[1] |
In Vitro | Some Salicylanilides and salicylamides could inhibit HIV virus by targeting of HIV-1 integrase or reverse transcriptase. Hepatitis C virus is another virus, which can be potentially afflicted by Salicylanilides on the level of two enzymes-NS3 protease and NS5B RNA polymerase[1]. |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 294.3±23.0 °C at 760 mmHg |
Melting Point | 136-138 °C(lit.) |
Molecular Formula | C13H11NO2 |
Molecular Weight | 213.232 |
Flash Point | 131.8±22.6 °C |
Exact Mass | 213.078979 |
PSA | 49.33000 |
LogP | 3.27 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.676 |
Water Solubility | SLIGHTLY SOLUBLE |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
Symbol |
GHS07, GHS09 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335-H400 |
Precautionary Statements | P261-P273-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S37/39 |
RIDADR | UN 3077 9 / PGIII |
WGK Germany | 2 |
RTECS | VN7850000 |
HS Code | 29242995 |
HS Code | 2924299090 |
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Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |