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CAS No.: | 91-56-5 |
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Name: | Isatin |
Molecular Structure: | |
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Formula: | C8H5NO2 |
Molecular Weight: | 147.133 |
Synonyms: | Indole-2,3-dione(8CI);2,3-Dihydro-1H-indole-2,3-dione;2,3-Dihydroindole-2,3-dione;2,3-Diketoindoline;2,3-Dioxo-2,3-dihydroindole;2,3-Dioxoindoline;2,3-Indolindione;2,3-Indolinedione;Isatic acid lactam;Isatin;Isatine;Isatinic acid anhydride;NSC 9262;Pseudoisatin;o-Aminobenzoylformic anhydride; |
EINECS: | 202-077-8 |
Density: | 1.367 g/cm3 |
Melting Point: | 193-195 °C (dec.)(lit.) |
Boiling Point: | 360.3 °C at 760 mmHg |
Flash Point: | 171.7 °C |
Solubility: | Soluble in water (1.9 g/L at 20°C). |
Appearance: | yellow to reddish crystalline solid |
Hazard Symbols: |
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Risk Codes: | 36/37/38-20/21/22 |
Safety: | 26-36-24/25 |
PSA: | 46.17000 |
LogP: | 0.95940 |
hydroxyimino-N-phenylacetamide
indole-2,3-dione
Conditions | Yield |
---|---|
With sulfuric acid at 20 - 30℃; for 1.66667h; Temperature; | 99% |
With sulfuric acid at 70℃; for 0.00277778h; Microwave irradiation; | 85% |
With sulfuric acid at 65 - 90℃; for 0.5h; | 81.3% |
indole-2,3-dione
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran; water at 20℃; for 5h; | 99% |
indole-2,3-dione
Conditions | Yield |
---|---|
With ozone In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide at 70℃; for 24h; Solvent; Temperature; Large scale; | 98.2% |
With potassium dichromate; sulfuric acid In water at 43℃; for 1.5h; Cooling; | 90% |
With potassium dichromate; sulfuric acid In water at 43℃; for 1.5h; | 90% |
With potassium dichromate; sulfuric acid In water at 43℃; for 1.5h; Cooling; | 90% |
With potassium dichromate; sulfuric acid In water |
3,3-dibromo-1-methoxy-2-oxindole
indole-2,3-dione
Conditions | Yield |
---|---|
With methanol Heating; | 98% |
Conditions | Yield |
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With oxygen; Rose Bengal lactone In water; N,N-dimethyl-formamide for 48h; Inert atmosphere; Irradiation; | 98% |
Conditions | Yield |
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With oxygen; copper(II) acetate monohydrate; potassium carbonate In N,N-dimethyl-formamide at 50℃; under 760.051 Torr; for 0.5h; | 95% |
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; oxygen In acetonitrile at 20℃; for 2h; Reagent/catalyst; Solvent; | 94% |
With tert.-butylhydroperoxide In decane; acetonitrile at 80℃; for 0.285h; Catalytic behavior; Flow reactor; Green chemistry; | 90% |
Conditions | Yield |
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With copper(I) bromide dimethylsulfide complex In tetrahydrofuran for 16h; Inert atmosphere; Reflux; | A 89% B 8% |
Conditions | Yield |
---|---|
With iron(III) chloride hexahydrate In acetonitrile at 100℃; Sealed tube; | A 88% B 89% |
3-Iodo-1H-indole
indole-2,3-dione
Conditions | Yield |
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With N-iodo-succinimide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 25 - 35℃; for 6h; | 89% |
N-(phenylthio)succinimide
C
indole-2,3-dione
Conditions | Yield |
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With dihydroquinine In dichloromethane at -70℃; for 12h; Reagent/catalyst; enantioselective reaction; | A n/a B 88% C 7% |
With C29H44N3O3P In tetrahydrofuran at -70℃; for 84h; Reagent/catalyst; enantioselective reaction; | A n/a B 20% C 71% |
IUPAC: 1H-indole-2,3-dione
CAS:91-56-5
The Molecular formula of INDOLE-2,3-DIONE(91-56-5):C8H5NO2
The Molecular Weight of INDOLE-2,3-DIONE(91-56-5):147.13
Synonyms:Isatin;TIMTEC-BB SBB009100;O-AMINOPHENYLGLYOXALIC LACTIM;O-AMINOBENZOYLFORMIC ACID;O-AMINOBENZOYLFORMIC ANHYDRIDE;AKOS BBS-00003223;2,3-DIKETOINDOLINE;2,3-DIHYDROINDOLE-2,3-DIONE;2,3-INDOLEDIONE
EINECS:202-077-8
Density:1.367g/cm3
Melting Point:198-204oC (Decomposes)(lit.)
Boiling Point:360.3oC at 760 mmHg
Flash Point:220oC
Solubility:Slightly soluble SOLVENT AUTOIGNITION
Appearance:yellow to reddish crystalline solid
liansport Information:25kgs
Product Categories:Intermediates;Heterocyclic Compounds;Indoles;Simple Indoles
Mol File:91-56-5.mol
storage temp.:Store at RT.
Decomposition:194oC
Merck:14,5104
BRN:383659
INDOLE-2,3-DIONE(91-56-5) is an indole derivative. In 1841, Erdman and Laurent first obtained the compound as a product from the oxidation of indigo dye by nitric acid and chromic acids. The compound is found in many plants.Schiff bases of INDOLE-2,3-DIONE are investigated for their pharmaceutical properties.It was observed that it forms a blue dye if it is mixed with sulfuric acid and crude benzene. The formation of the blue indophenin was long believed to be a reaction with benzene. Victor Meyer was able to isolate the substance responsible for this reaction from benzene. This new heterocyclic compound was thiophene.
1. | orl-rat LDLo:5 g/kg | IJPPAZ Indian Journal of Physiology and Pharmacology. 6 (1962),145. | ||
2. | orl-mus LD50:300 mg/kg | NYKZAU Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. 55 (1959),1514. | ||
3. | ipr-mus LD50:563 mg/kg | PCJOAU Pharmaceutical Chemistry Journal (English Translation). Translation of KHFZAN. 15 (1981),858. |
Poison by ingestion. Moderately toxic by intraperitoneal route. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx. See also ANHYDRIDES.
Safty informations about INDOLE-2,3-DIONE(91-56-5):
Hazard Codes:Xi,Xn
Risk Statements:36/37/38-20/21/22
36/37/38 (Irritating to the eyes ,piratory system and skin)
20/21/22(Harmful by inhalation, in contact with skin and if swallowed)
Safety Statements:26-36-24/25
26 (In case of contact with eyes,rinse immediately with plenty of water and seek medical advice)
36 (Wear suitable protective clothing)
24/25(Avoid contact with skin and eyes)
WGK Germany:1
RIDADR:2811
RTECS:NL7873000
HazardClass:6.1(b)
PackingGroup:III
HS Code:29337900