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BENZO[CD]INDOL-2(1H)-ONE

benz(cd)indol-2(1H)-one

CAS: 130-00-7

Molecular Formula: C11H7NO

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BENZO[CD]INDOL-2(1H)-ONE - Names and Identifiers

Name benz(cd)indol-2(1H)-one
Synonyms naphtholactam
Naphthostyril
1,8-Naphtholactam
1,8-Naphthostyril
1,8-Naphtaholactam
1,8-Naphthaolactam
2H-benzo[f]indol-2-one
Benz[cd]indol-2(1H)-one
BENZ[CD]INDOL-2(1H)-ONE
2(1h)-perinaphthazolone
benz(cd)indol-2(1H)-one
Benz(CD)Indol-2-(1H)-One
BENZO[CD]INDOL-2(1H)-ONE
benzo[cd]indol-2(1H)-one
1,8-Naphthaleneformylimine
Naphthostyril 1,8-Naphtholactam
CAS 130-00-7
EINECS 204-973-4
InChI InChI=1/C11H7NO/c13-11-8-5-1-3-7-4-2-6-9(12-11)10(7)8/h1-6H,(H,12,13)
InChIKey GPYLCFQEKPUWLD-UHFFFAOYSA-N

BENZO[CD]INDOL-2(1H)-ONE - Physico-chemical Properties

Molecular FormulaC11H7NO
Molar Mass169.18
Density1.1616 (rough estimate)
Melting Point173-178°C(lit.)
Boling Point298.46°C (rough estimate)
Flash Point128.9°C
Solubility methanol: soluble25mg/mL, clear to slightly hazy, yellow to brown
Vapor Presure0.61-7.2Pa at 100-130℃
AppearanceWhite crystal
ColorLight orange to Yellow to Green
pKa13.27±0.20(Predicted)
Storage ConditionSealed in dry,Room Temperature
Refractive Index1.4900 (estimate)
MDLMFCD00009748
Physical and Chemical PropertiesFine needle-like crystals, melting point 180-181 °c. Soluble in boiling water, slightly soluble in ether.
UseIntermediates for the synthesis of vat dyes and organic pigments

BENZO[CD]INDOL-2(1H)-ONE - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk Codes22 - Harmful if swallowed
Safety Description24/25 - Avoid contact with skin and eyes.
WGK Germany2
RTECSDE3202000
HS Code29337900

BENZO[CD]INDOL-2(1H)-ONE - Upstream Downstream Industry

Raw Materials1,8-Naphthalimide

BENZO[CD]INDOL-2(1H)-ONE - Reference Information

LogP2.5 at 24℃ and pH6.6
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
Uses Intermediates for the synthesis of vat dyes and organic pigments
Dye intermediates
Photoinduced Fries rearrangement reaction reagent; Preparation of powerful anti-tumor agent reagents; Used for the synthesis of thymidylate synthase inhibitors
production method obtained by rearranging 1,8-naphthalimide. Add water, sodium hydroxide solution and caustic potassium solution in the reaction pot, add sodium hypochlorite and diffusion agent NNO while stirring, add 1,8-naphthalimide at 30 ℃, and keep the temperature at 28-30 ℃ for 2.5h. Maintain excess sodium hypochlorite during the reaction. At the end of heat preservation, excess sodium hypochlorite was eliminated with sodium sulfite, and adjusted to 9.5-10 with hydrochloric acid. The unreacted naphthalene diimide was filtered out, the filtrate was below 40 ℃, and the pH was 2-3 with hydrochloric acid. Heat to 80-85 ℃, keep the temperature for half an hour, and close the loop. Cool to 60 ℃, filter and wash to obtain 1,8-naphthalene imide.
Last Update:2024-04-09 20:49:11
BENZO[CD]INDOL-2(1H)-ONE
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View History
BENZO[CD]INDOL-2(1H)-ONE
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Raw Materials for BENZO[CD]INDOL-2(1H)-ONE
1,8-Naphthalimide
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