Page last updated: 2024-12-07

2-amino-5-chlorophenol

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

Description

2-amino-5-chlorophenol: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

2-amino-5-chlorophenol : Phenol carrying amino and chloro substituents at positions 2 and 5 respectively. It is part of the degradation pathway of 4-chloronitrobenzene, CHEBI:34399. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID91591
CHEBI ID75051
SCHEMBL ID103329
MeSH IDM0261595

Synonyms (35)

Synonym
2-amino-5-chlorophenol, 97%
2-amino-5-chlorophenol
fzcqmirjcgwwcl-uhfffaoysa-
inchi=1/c6h6clno/c7-4-1-2-5(8)6(9)3-4/h1-3,9h,8h2
28443-50-7
A819448
ec 249-020-3
einecs 249-020-3
6vk2h53lqn ,
unii-6vk2h53lqn
phenol, 2-amino-5-chloro-
5-chloro-2-aminophenol
2-hydroxy-4-chloroaniline
CHEBI:75051
4-chloro-2-hydroxyaniline
5-chloro-o-aminophenol
AKOS008967300
FT-0601050
C20669
PS-6280
BBL018708
AM20060326
SCHEMBL103329
2-amino-5-chloro-phenol
FZCQMIRJCGWWCL-UHFFFAOYSA-N
DTXSID6067385
mfcd02093863
W-107043
AC-8704
Q27145090
3-chloro-6-aminophenol
STL194297
CS-W019030
CCG-302530
EN300-98784
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (3)

ClassDescription
phenolsOrganic aromatic compounds having one or more hydroxy groups attached to a benzene or other arene ring.
primary amino compoundA compound formally derived from ammonia by replacing one hydrogen atom by an organyl group.
monochlorobenzenesAny member of the class of chlorobenzenes containing a mono- or poly-substituted benzene ring in which only one substituent is chlorine.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (2)

PathwayProteinsCompounds
4-chloronitrobenzene degradation620
chlorzoxazone degradation17

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's3 (50.00)18.2507
2000's2 (33.33)29.6817
2010's1 (16.67)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: 25.12

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 Index25.12 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.31 (4.65)
Search Engine Demand Index20.59 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (25.12)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]