Page last updated: 2024-11-05

2,7-dinitrofluorene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

2,7-Dinitrofluorene is a yellow solid compound with the formula C13H6N2O4. It is a nitro derivative of fluorene and is used in the synthesis of various organic compounds. 2,7-Dinitrofluorene is known to exhibit antimicrobial activity against certain bacteria and fungi. It is also used as a precursor in the synthesis of dyes and pigments. Its synthesis involves nitration of fluorene with concentrated nitric acid. The compound is also studied in the field of materials science due to its potential applications in organic electronics and optoelectronic devices. '

Cross-References

ID SourceID
PubMed CID21502
CHEMBL ID167848
SCHEMBL ID987760
MeSH IDM0225838

Synonyms (34)

Synonym
AC-4880
AKOS005443889
nsc5180
2,7-dinitrofluorene ,
wln: l b656 hhj enw knw
9h-fluorene,7-dinitro-
5405-53-8
nsc-5180
fluorene,7-dinitro-
fluorene, 2,7-dinitro-
9h-fluorene, 2,7-dinitro-
einecs 226-457-8
brn 2057852
ccris 2909
nsc 5180
OPREA1_216229
2,7-dinitro-9h-fluorene ,
STK367081
2,7-dinitrofluorene, 97%
D0834
CHEMBL167848
4-05-00-02153 (beilstein handbook reference)
unii-d67mt7zuy3
d67mt7zuy3 ,
A829933
SCHEMBL987760
2,7-dinitro-9h-fluorene #
IHZCVUBSTYOFSJ-UHFFFAOYSA-N
Q-101168
mfcd00001121
DTXSID8075253
2,7-dinitrofluoren
AS-33146
AMY2555
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID23442Partition coefficient (logP)1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Structure-activity relationship of mutagenic aromatic and heteroaromatic nitro compounds. Correlation with molecular orbital energies and hydrophobicity.
AID200690Mutagenic activity in an Ames test on Salmonella Typhimurium TA98; Activity is log of revertants/nmol1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Structure-activity relationship of mutagenic aromatic and heteroaromatic nitro compounds. Correlation with molecular orbital energies and hydrophobicity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's3 (42.86)18.2507
2000's3 (42.86)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 17.41

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index17.41 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.31 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (17.41)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (14.29%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (85.71%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]