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4-nitro-1H-indoIe
4-nitro-1H-indole-3-carbaldehyde
4-nitro-1H-indoIe
Conditions | Yield |
---|---|
With hydrogenchloride In methanol for 1.5h; Heating; | 99% |
methyl 2-hydroxy-2-(4-nitroindol-1-yl)-acetate
4-nitro-1H-indoIe
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In methanol; water for 0.0833333h; Heating; | 94.5% |
methyl 2-(4-nitroindole-1-yl)oxyacetate
4-nitro-1H-indoIe
Conditions | Yield |
---|---|
With triethylamine In methanol for 16h; Ambient temperature; | 94.3% |
2,6-dinitrostyrene
4-nitro-1H-indoIe
Conditions | Yield |
---|---|
With triphenylphosphine; palladium diacetate In acetonitrile under 3040 Torr; for 26h; Heating; | 89% |
With carbon monoxide; palladium diacetate; triphenylphosphine In acetonitrile at 90℃; under 3051.25 Torr; for 50h; | 89% |
4-nitro-1H-indole-3-carbaldehyde
sodium cyanide
A
4-nitro-1H-indoIe
B
4-nitro-3-indoleacetonitrile
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol; formamide at 100℃; for 5h; | A 2% B 88% C 9% |
1-hydroxy-4-nitroindole
ethyl bromoacetate
A
4-nitro-1H-indoIe
B
methyl 2-hydroxy-2-(4-nitroindol-1-yl)-acetate
C
methyl 2-(4-nitroindole-1-yl)oxyacetate
Conditions | Yield |
---|---|
With triethylamine In methanol for 43h; Ambient temperature; | A 59.2% B 20% C 14.4% |
With triethylamine In methanol Product distribution; Ambient temperature; different reaction time; |
3-nitro-trans-2-[β-(dimethylamino)vinyl]-nitrobenzene
A
4-amino-1H-indole
B
4-nitro-1H-indoIe
C
1-hydroxy-4-nitroindole
D
1-hydroxy-4-nitrooxyindole
Conditions | Yield |
---|---|
With titanium(III) chloride In water; acetic acid for 0.116667h; Ambient temperature; | A 2.8% B 13.1% C 56.8% D 15.9% |
With titanium(III) chloride In methanol for 0.116667h; Ambient temperature; | A 3.6% B 31.3% C 47.3% D 5.6% |
With titanium(III) chloride In N,N-dimethyl-formamide for 0.116667h; Product distribution; Ambient temperature; investigation of the synthesis and stability of the 4-substituted 1-hydroxy-indoles; | A 41.8% B 6.3% C 21.9% D 1.3% |
potassium cyanide
4-nitrogramine
A
4-nitro-1H-indoIe
B
4-nitro-3-indoleacetonitrile
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide for 1.5h; Heating; | A 9.9% B 55.9% |
In water; N,N-dimethyl-formamide for 2h; Heating; | A 24.6% B 50.7% |
Conditions | Yield |
---|---|
With palladium diacetate; trifluoroacetic acid at 100℃; for 4h; | 52% |
The 4-Nitroindole, with the CAS registry number 4769-97-5, has the IUPAC name of 4-nitro-1H-indole. For being a kind of yellow crystalline solid, it is usually applied as the organic synthesis reagent and its product categories are including blocks; IndolesOxindoles; NitroCompounds; Indoles and derivatives; Indole; Indole Derivatives; Indoles; Simple Indoles; Building Blocks; Heterocyclic Building Blocks; Heterocyclic Building Blocks.
The characteristics of this chemical are as follows: (1)#H bond acceptors: 4; (2)#H bond donors: 1; (3)#Freely Rotating Bonds: 1; (4)Polar Surface Area: 50.75; (5)Index of Refraction: 1.723; (6)Molar Refractivity: 45.07 cm3; (7)Molar Volume: 113.7 cm3; (8)Polarizability: 17.86 ×10-24 cm3; (9)Surface Tension: 67.7 dyne/cm; (10)Density: 1.425 g/cm3; (11)Flash Point: 173.1 °C; (12)Enthalpy of Vaporization: 58.46 kJ/mol; (13)Boiling Point: 362.6 °C at 760 mmHg; (14)Vapour Pressure: 3.98E-05 mmHg at 25°C; (15)Exact Mass: 162.042927; (16)MonoIsotopic Mass: 162.042927; (17)Topological Polar Surface Area: 61.6; (18)Heavy Atom Count: 12; (19)Complexity: 190.
When you are dealing with this chemical, you should be very careful. For one thing, it is irritant which may cause inflammation to the skin or other mucous membranes. For another thing, it is harmful which may cause damage to health, and it will have possible risk of irreversible effects. Therefore, you should take the following instructions. Wear suitable protective clothing and gloves, and if in case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
Additionally, you could convert the following datas into the molecular structure:
(1)Canonical SMILES: C1=CC2=C(C=CN2)C(=C1)[N+](=O)[O-]
(2)InChI: InChI=1S/C8H6N2O2/c11-10(12)8-3-1-2-7-6(8)4-5-9-7/h1-5,9H
(3)InChIKey: LAVZKLJDKGRZJG-UHFFFAOYSA-N