1-amino-2-naphthol

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

1-amino-2-naphthol is a versatile organic compound that is a key intermediate in the synthesis of various dyes, pigments, and pharmaceuticals. It exhibits a strong reducing ability, making it useful as a developer in photography. Research on 1-amino-2-naphthol explores its chemical reactivity, synthesis pathways, and potential applications in various industries. The compound is also studied for its potential antioxidant and antimicrobial properties.'

Cross-References

ID Source	ID
PubMed CID	14535
SCHEMBL ID	144625
MeSH ID	M0239535

Synonyms (42)

Synonym
BB 0245398
1-amino-naphthalen-2-ol
2834-92-6
.alpha.-amino-.beta.-naphthol
2-naphthalenol, 1-amino-
1-amino-2-hydroxynaphthalene
nsc7938
2-hydroxy-1-aminonaphthalene
1-amino-2-naphthol ,
2-naphthol, 1-amino-
nsc-7938
EC-000.1432
1-aminonaphthalen-2-ol
STK397753
AKOS000108846
KUC106766N
ksc-11-229-01
STL040664
1-ammonionaphthalen-2-olate
95609-86-2
alpha-amino-beta-naphthol
mb1zpm5m0z ,
nsc 7938
unii-mb1zpm5m0z
einecs 220-606-0
A819422
BBL012066
FT-0634511
2-naphthalenol, amino-
SCHEMBL144625
1-amino-2-naphthalenol
1-amino 2-hydroxynapthalene
1-amino 2-hydroxy naphthalene
1-amino 2-hydroxy napthalene
1-aminonaphthalene-2-ol
mfcd00628991
2-hydroxy-1-naphthylamine
VS-03191
2-[alpha-(2,4-ditert-amylphenoxy)butyramide]-4,6-dichloro-5-ethylphenol
Q27283782
DTXSID20883897
CAA83492

Research Excerpts

Dosage Studied

Excerpt	Relevance	Reference
" Compared with conventional anaerobic biological methods, the required dosage of organic cosubstrate was significantly reduced in the BES."	( Decolorization of azo dyes in bioelectrochemical systems. Keller, J; Mu, Y; Rabaey, K; Rozendal, RA; Yuan, Z, 2009)	0.35

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	1 (12.50)	18.7374
1990's	1 (12.50)	18.2507
2000's	3 (37.50)	29.6817
2010's	3 (37.50)	24.3611
2020's	0 (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: 39.31

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 strong demand-to-supply ratio for research on this compound.

Metric	This Compound (vs All)
Research Demand Index	39.31 (24.57)
Research Supply Index	2.20 (2.92)
Research Growth Index	4.80 (4.65)
Search Engine Demand Index	50.91 (26.88)
Search Engine Supply Index	2.00 (0.95)

This Compound (39.31)

All Compounds (24.57)

Study Types

Publication Type	This drug (%)	All Drugs (%)
Trials	0 (0.00%)	5.53%
Reviews	0 (0.00%)	6.00%
Case Studies	0 (0.00%)	4.05%
Observational	0 (0.00%)	0.25%
Other	8 (100.00%)	84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Substance	Relationship Strength	Studies	Classes	Roles
methane Methane: The simplest saturated hydrocarbon. It is a colorless, flammable gas, slightly soluble in water. It is one of the chief constituents of natural gas and is formed in the decomposition of organic matter. (Grant & Hackh's Chemical Dictionary, 5th ed). methane : A one-carbon compound in which the carbon is attached by single bonds to four hydrogen atoms. It is a colourless, odourless, non-toxic but flammable gas (b.p. -161degreeC).	2.11	1	alkane; gas molecular entity; mononuclear parent hydride; one-carbon compound	bacterial metabolite; fossil fuel; greenhouse gas
4-nitrophenol 4-nitrophenol: RN given refers to parent cpd. mononitrophenol : A nitrophenol that is phenol carrying a single nitro substituent at unspecified position.. 4-nitrophenol : A member of the class of 4-nitrophenols that is phenol in which the hydrogen that is para to the hydroxy group has been replaced by a nitro group.	2.11	1	4-nitrophenols	human xenobiotic metabolite; mouse metabolite
aniline [no description available]	2.45	2	anilines; primary arylamine
2-toluidine 2-toluidine: RN given refers to parent cpd. o-toluidine : An aminotoluene in which the amino substituent is ortho to the methyl group.	2.03	1	aminotoluene	carcinogenic agent
2,4-xylidine 2,4-xylidine: RN given refers to parent cpd; structure. 2,4-dimethylaniline : A primary arylamine that is aniline in which the hydrogens at the 2- and 4-positions are replaced by methyl groups. A clear to yellow liquid, it is used in production of certain dyes, pesticides and other chemicals.	2.03	1	dimethylaniline; primary arylamine
3,4-dichloroaniline 3,4-dichloroaniline : A dichloroaniline having the two chloro-substituents at the 3- and 4-positions.	2.11	1	dichloroaniline	epitope; xenobiotic
3-nitroaniline 3-nitroaniline: used as a sole source of nitrogen , carbon and energy	2.11	1
4-nitroaniline [no description available]	2.03	1	nitroaniline	bacterial xenobiotic metabolite
4-phenylenediamine 4-phenylenediamine: agent hair dye responsible for contact dermatitis; RN given refers to parent cpd. 1,4-phenylenediamine : A phenylenediamine in which the amino functions are at positions 1 and 4 of the benzene nucleus.	2.06	1	phenylenediamine	allergen; dye; hapten; reagent
pyrroles 1H-pyrrole : A tautomer of pyrrole that has the double bonds at positions 2 and 4.. pyrrole : A five-membered monocyclic heteroarene comprising one NH and four CH units which forms the parent compound of the pyrrole group of compounds. Its five-membered ring structure has three tautomers. A 'closed class'.. azole : Any monocyclic heteroarene consisting of a five-membered ring containing nitrogen. Azoles can also contain one or more other non-carbon atoms, such as nitrogen, sulfur or oxygen.	2.11	1	pyrrole; secondary amine
2-naphthol 2-naphthol: RN given refers to parent cpd. 2-naphthol : A naphthol carrying a hydroxy group at position 2.. naphthols : Any hydroxynaphthalene derivative that has a single hydroxy substituent.	8.5	8	naphthol	antinematodal drug; genotoxin; human urinary metabolite; human xenobiotic metabolite; mouse metabolite; radical scavenger
2,4-dichloroaniline 2,4-dichloroaniline: RN given refers to parent cpd. 2,4-dichloroaniline : A dichloroaniline carrying chloro substituents at positions 2 and 4.	2.11	1	dichloroaniline
1-phenylazo-2-naphthol 1-phenylazo-2-naphthol: RN given refers to cpd without isomeric designation	2.46	2
sudan red [no description available]	2.46	2
d.c. red no. 9 [no description available]	1.98	1
para red para red: a dye; structure in first source	2.07	1
sudan iii sudan III: structure in first source. Sudan III : A bis(azo) compound that is 2-naphthol substituted at position 1 by a 4-{[(2-methylphenyl)diazenyl]phenyl}diazenyl group. A fat-soluble dye predominantly used for demonstrating triglycerides in frozen sections, but which may also stain some protein bound lipids in paraffin sections.	2.75	3	azobenzenes; bis(azo) compound; naphthols	carcinogenic agent; fluorochrome; histological dye
nitrophenols Nitrophenols: PHENOLS carrying nitro group substituents.	2.11	1
flavin mononucleotide Flavin Mononucleotide: A coenzyme for a number of oxidative enzymes including NADH DEHYDROGENASE. It is the principal form in which RIBOFLAVIN is found in cells and tissues.	1.98	1
2-naphthol orange 2-naphthol orange: structure; see also record for C.I. Solvent Orange 2	2.06	1

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