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638854

Sigma-Aldrich

7-Nitroindole

97%

Synonym(s):

NSC 69874

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About This Item

Empirical Formula (Hill Notation):
C8H6N2O2
CAS Number:
6960-42-5
Molecular Weight:
162.15
MDL number:
MFCD00005683
UNSPSC Code:
12352100
PubChem Substance ID:
24882983
NACRES:
NA.22

Assay

97%

form

solid

mp

94-98 °C (lit.)

SMILES string

[O-][N+](=O)c1cccc2cc[nH]c12

InChI

1S/C8H6N2O2/c11-10(12)7-3-1-2-6-4-5-9-8(6)7/h1-5,9H

InChI key

LZJGQIVWUKFTRD-UHFFFAOYSA-N

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Application

Reactant for preparation of:
  • Protein kinase inhibitors
  • Potential fructose 1,6-bisphosphatase inhibitors
  • Factor Xa inhibitors
  • Antagonist of the mineralocorticoid receptor
  • Antitumor sulfonamides
  • Inosine monophosphate dehydrogenase (IMPDH) inhibitors
  • Subtype-selective cyclooxygenase (COX) inhibitors
  • Thrombin protease-activated receptor (PAR-1) ligands

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Chaitany Jayprakash Raorane et al.
Biomolecules, 10(8) (2020-08-23)
Multi-drug resistant Acinetobacter baumannii is well-known for its rapid acclimatization in hospital environments. The ability of the bacterium to endure desiccation and starvation on dry surfaces for up to a month results in outbreaks of health care-associated infections. Previously, indole

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