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Molecule
ID:12050
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₆N₂O₂
Molecular Mass
162.14544
Exact Mass
162.04292744
Charge
0
InChI
InChI=1S/C8H6N2O2/c11-10(12)8-3-1-2-7-6(8)4-5-9-7/h1-5,9H
InChIKey
LAVZKLJDKGRZJG-UHFFFAOYSA-N
Canonic Smiles
[O-][N+](=O)c1cccc2c1cc[nH]2
Isomeric Smiles
c1c[nH]c2c1c(ccc2)[N+](=O)[O-]
Calculated Properties
JChem
Acid pKa
13.255104
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
2.011992
LogD (pH = 7.4)
2.0119915
Log P
2.011992
Molar Refractivity
43.465
Polarizability
17.394144
Polar Surface Area
58.93
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
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Commercial Catalog
•
Academic Data
Names and Identifiers
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IUPAC Traditional name
•
Synonyms
•
IUPAC name
Registration numbers
Properties
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Product Information
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Safety Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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TRC
References
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PubChem Literature
•
From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
009071
Apollo Scientific
OR7858
Alfa Aesar
L09177
InterBioScreen
BB_SC-10870
Maybridge
RH01152
Sigma Aldrich
269964
TRC
N496275
Enamine
EN300-78054
Bide Pharmatech
BD5991
A&J Pharmtech
AJA-O38436
Academic Data
PubChem
145766
Names and Identifiers
IUPAC Traditional name
4-nitro-1H-indole
Synonyms
4-Nitroindole
4-nitro-1H-indole
4-Nitroindole
4-硝基吲哚
4-Nitro-1H-indole 97%
4-Nitro-1H-indole
IUPAC name
4-nitro-1H-indole
Registration numbers
CAS Number
4769-97-5
PubChem SID
160975357
24856183
PubChem CID
145766
MDL Number
MFCD00010056
Beilstein Number
136022
Molecule Details
Sigma Aldrich
269964
Packaging
1 g in glass bottle
500 mg in glass bottle
Application
Reactant for preparation of:
• Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Meridianin derivatives as protein kinase (PKC) inhibitors and vitro antiproliferative agents2
• Anti-angiogenic agents3
• Sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors for the management of hyperglycemia in diabetes4
• Biologically active indoles5
• CGRP receptor antagonists6
• Nucleosides7
• CB2 cannabinoid receptor ligands8
TRC
N496275
4-Nitroindole is an intermediate for the preparation of indole compounds useful in treatment of pain, inflammation.
References
PubChem Literature
From Data Sources
•
Leclerc, S., et al.: J. Biol. Chem., 276, 251 (2001)
•
Alonso, M., et al.: Curr. Med. Chem., 11, 755 (2001)
•
Meijer, L., et al.: Chem. Biol., 10, 1255 (2001)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
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PubChem SID
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PubChem CID
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MDL Number
•
Beilstein Number
Properties
Product Information
Purity
98%
Source
97%
Source
95%
Source
Empirical Formula (Hill Notation)
C8H6N2O2
Source
Certificate of Analysis
Download link
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Storage Warning
IRRITANT, IRRITANT-HARMFUL
Source
Irritant
Source
TSCA Listed
false
Source
否
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Physical Property
Melting Point
205-207°C
Source
205-207 °C(lit.)
Source
205-207°C
Source
206 - 207°C
Source
202-207°C
Source
Solubility
Methanol
Source
Ethyl Acetate
Source
Acetone
Source
Dichloromethane
Source
Yellow Crystalline Solid
Source
2.235
Source
Apperance
Hydrophobicity(logP)