Basic information Safety Supplier Related

6-Nitroindoline

Basic information Safety Supplier Related

6-Nitroindoline Basic information

Product Name:
6-Nitroindoline
Synonyms:
  • 2,3-DIHYDRO-6-NITRO-(1H)-INDOLE
  • 6-nitro-indolin
  • 6-Nitroindzole
  • 6-NITROINDOLINE
  • 6-NITRO-2,3-DIHYDROINDOLE
  • 6-NITRO-2,3-DIHYDRO-1H-INDOLE
  • 6-NITRO-2,3-DIHYDRO-1H-INDOLE HYDROCHLORIDE
  • 6-NITROINDOLINE, 98+%
CAS:
19727-83-4
MF:
C8H8N2O2
MW:
164.16
EINECS:
243-257-6
Product Categories:
  • Building Blocks
  • C7 to C9
  • Indoles and derivatives
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Heterocyclic Building Blocks
  • Indoles
Mol File:
19727-83-4.mol
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6-Nitroindoline Chemical Properties

Melting point:
67-69 °C (lit.)
Boiling point:
291.62°C (rough estimate)
Density 
1.2739 (rough estimate)
refractive index 
1.6000 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
Crystalline Powder or Crystals
pka
3.39±0.20(Predicted)
color 
Orange or red
BRN 
156434
CAS DataBase Reference
19727-83-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
RTECS 
NM1950000
Hazard Note 
Irritant
HS Code 
29339900
Toxicity
mouse,LD50,intravenous,56mg/kg (56mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#00607,

MSDS

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6-Nitroindoline Usage And Synthesis

Chemical Properties

orange crystalline powder or red crystals

Uses

• ;Reactant for preparation of 2-[(2,3-Dihydro-1H-indol-1-yl)methyl]melatonin analogs as novel MT2-selective melatonin receptor antagonists1• ;Reactant for synthesis of isoindigo and azaisoindigo glycosides as anticancer agents2• ;Reactant for preparation of arylfurancarboxamides with Nav1.8 voltage-gated Na channel blocking/analgesic activities3• ;Reactant for preparation of bicyclic benzamides as 5-HT1 receptor agonists4• ;Reactant for preparation of antiarrhythmic benzopyrans5• ;Reactant for preparation of 5-HT2C/2B receptor antagonists6

Uses

  • Reactant for preparation of 2-[(2,3-Dihydro-1H-indol-1-yl)methyl]melatonin analogs as novel MT2-selective melatonin receptor antagonists
  • Reactant for synthesis of isoindigo and azaisoindigo glycosides as anticancer agents
  • Reactant for preparation of arylfurancarboxamides with Nav1.8 voltage-gated Na channel blocking/analgesic activities
  • Reactant for preparation of bicyclic benzamides as 5-HT1 receptor agonists
  • Reactant for preparation of antiarrhythmic benzopyrans
  • Reactant for preparation of 5-HT2C/2B receptor antagonists

6-NitroindolineSupplier

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