4,7-Dichloroisatin

4,7-Dichloroisatin Basic information
Product Name:4,7-Dichloroisatin
Synonyms:4,7-DICHLOROINDOLINE-2,3-DIONE;4,7-DICHLOROISATIN;4,7-dichloro-2,3-dihydro-1H-indole-2,3-dione;4,7-dichloro-1H-indole-2,3-dione;4,7-Dichloroisatin,99%;BUTTPARK 50\07-81;4,7-Dichloroindole-2,3-dione;1H-Indole-2,3-dione, 4,7-dichloro-
CAS:18711-13-2
MF:C8H3Cl2NO2
MW:216.02
EINECS:622-637-9
Product Categories:Indoles and derivatives;Halogenated Heterocycles;Heterocyclic Building Blocks;Indoles;IndolesBuilding Blocks
Mol File:18711-13-2.mol
4,7-Dichloroisatin Structure
4,7-Dichloroisatin Chemical Properties
Melting point 250-252 °C(lit.)
density 1.643±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka8.38±0.20(Predicted)
color Light yellow to Brown
BRN 168731
InChIInChI=1S/C8H3Cl2NO2/c9-3-1-2-4(10)6-5(3)7(12)8(13)11-6/h1-2H,(H,11,12,13)
InChIKeyNUXYYWOWNFEMNH-UHFFFAOYSA-N
SMILESN1C2=C(C(Cl)=CC=C2Cl)C(=O)C1=O
CAS DataBase Reference18711-13-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 22-36
Safety Statements 26-36
WGK Germany 3
HS Code 29337900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
4,7-Dichloroisatin Usage And Synthesis
Chemical Propertiesorange flakes
UsesUsed as an intermediate in organic synthesis.
SynthesisTo a mixture of 2,5-Dichloroaniline (1.02 g, 7.84 mmol), anhydrous sodium sulfate (8.94 g, 62.71 mmol), hydroxylamine hydrochloride (2.24 g, 31.35 mmol) and 1M hydrochloric acid (8.0 mL) in water (60 mL) is added chloral hydrate (1.58 g, 9.41 mmol) at room temperature. The resulting mixture is warmed to 55 °C and stirred for 6 hours. While the mixture is cooling to room temperature, solid precipitate is formed and collected by filtration, washed with water and dried under vacuum to yield the hydroxyliminoacetanilide intermediate, which is added in small portions to concentrated sulfuric acid (5.0 mL) that is preheated to 55 °C. The temperature of the reaction mixture is maintained at below 58 °C throughout the addition. After the addition is completed, the dark-colored mixture is heated to 80 °C for 10 minutes before cooling down to room temperature. The mixture is then poured into crushed ice, swirled, and left to stand for 30 minutes. 4,7-Dichloroisatin formed is collected by filtration, washed with water and dried under vacuum.
synthesis of 4,7-Dichloroisatin
4,7-Dichloroisatin Preparation Products And Raw materials
Preparation Products(+)-YK-4-279
(2-CHLOROPHENYL)ACETALDEHYDE 2-Chloro-6-methylaniline 4-CHLOROISATIN C-(1H-IMIDAZOL-2-YL)-METHYLAMINE 2',5'-DICHLOROACETANILIDE (2,5-DICHLORO-PHENYL)-ETHYL-AMINE 2',5'-Dichloroacetophenone 2-(3-Chlorophenyl)ethylamine 3’-Chloroacetophenone 4,5,7-trichloro-1H-indole-2,3-dione 2-AMINO-6-CHLOROTOLUENE HYDROCHLORIDE 3-Chloro-2-methylaniline 7-chloroindoline N-Methyl 3-chloro-2-methylaniline, HCl 2'-Chloroacetophenone 2-Amino-2'-chloroacetophenone 7-CHLORO-1H-INDAZOLE-3-CARBOXYLIC ACID 7-CHLOROISATIN

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