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Salicylanilide

Salicylanilide Basic information
Product Name:Salicylanilide
Synonyms:Aseptolan;ASK;Sherstat SLN;sherstatsln;Shirlan AG;Shirlan Extra;shirlanag;shirlanextra
CAS:87-17-2
MF:C13H11NO2
MW:213.23
EINECS:201-727-8
Product Categories:SALINIDOL;PHARMACEUTICAL INTERMEDIATES
Mol File:87-17-2.mol
Salicylanilide Structure
Salicylanilide Chemical Properties
Melting point 136-138 °C (lit.)
Boiling point 353.22°C (rough estimate)
density 1.1544 (rough estimate)
refractive index 1.5700 (estimate)
storage temp. Store below +30°C.
solubility H2O: slightly soluble
form buffered aqueous glycerol solution
pka7.11±0.10(Predicted)
color White to Almost white
PH7-7.5 (50g/l, H2O, 25℃)
Water Solubility SLIGHTLY SOLUBLE
Merck 14,8330
BRN 1108135
CAS DataBase Reference87-17-2(CAS DataBase Reference)
NIST Chemistry ReferenceBenzamide, 2-hydroxy-N-phenyl-(87-17-2)
EPA Substance Registry SystemSalicylanilide (87-17-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-36
RIDADR UN 3077 9 / PGIII
WGK Germany 2
RTECS VN7850000
Autoignition Temperature>300 °C
TSCA Yes
HS Code 29242995
MSDS Information
ProviderLanguage
N-Phenylsalicylamide English
SigmaAldrich English
ACROS English
ALFA English
Salicylanilide Usage And Synthesis
Chemical Propertiesgreyish-brownish powder
UsesAnti-mildew, fungicide.
Usesantipyretic, fungicide
UsesSalicylanilides are compounds of varying biological activity ranging from anti-inflammatory agents to antiviral and antimicrobial agents.
DefinitionChEBI: An amide of salicylic acid and of aniline; it is therefore both a salicylamide and an anilide.
General DescriptionSalicylanilide inhibited mycobacterial isocitrate lyase (ICL) and showed a significant antimycobacterial effect.
HazardToxic by ingestion, irritant to skin.
Salicylanilide Preparation Products And Raw materials
Raw materialsCarbon tetrachloride-->Methyl salicylate-->Phenyl salicylate
Preparation Products3,5,4'-TRIBROMOSALICYLANILIDE-->Benzamide,3,5-dichloro-N-(2,4-dichlorophenyl)-2-hydroxy-
Naphthol AS POLY(N-ISOPROPYL ACRYLAMIDE) 4'-chloro-5-bromo Salicylanilide SODIUM SALICYLANILIDE 5-CHLOROSALICYLANILIDE N-(2-ETHYLPHENYL)-3-HYDROXY-2-NAPHTHALENECARBOXAMIDE 2-Hydroxy-N-(4-hydroxyphenyl)-benzamide N-(2,6-dimethylphenyl)-2-hydroxybenzamide 2-[2-HYDROXY-3-(2,4-XYLYLCARBAMOYL)-1-NAPHTHYLAZO]PHENOL N-(2,3-Dihydro-2-oxo-1H-benzimidazol-5-yl)-3-hydroxy-2-naphthalenecarboxamide 3'-TRIFLUOROMETHYL-3,5-DIBROMO SALICYLANILIDE 3',4'-DICHLOROSALICYLANILIDE 10,11-DIHYDRODIBENZ[B,F][1,4]OXAZEPIN-11-ONE Salicylanilide,4’-bromo Salicylanilide, 3-propyl- (6CI) N-(4-chlorophenyl)-2-hydroxybenzamide NAPHTHOL AS ACETATE CHLOROPHOSPHONAZO III
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