Compounds > alpha-bromonaphthalene
Page last updated: 2024-12-05

alpha-bromonaphthalene

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

Alpha-bromonaphthalene is a synthetic organic compound that serves as a versatile building block in organic synthesis. It is a colorless to pale yellow solid with a pungent odor. The compound can be synthesized through electrophilic aromatic bromination of naphthalene using bromine and a catalyst such as iron or aluminum bromide. Alpha-bromonaphthalene is employed in the preparation of various organic molecules, including pharmaceuticals, dyes, and pesticides. Its reactivity and ability to undergo diverse chemical transformations make it a valuable tool in organic chemistry research. Studies involving alpha-bromonaphthalene explore its potential applications in drug discovery, material science, and other areas. The compound's unique properties, such as its ability to form stable carbon-carbon bonds and its compatibility with various reaction conditions, contribute to its significance in organic synthesis.'

Cross-References

ID SourceID
PubMed CID7001
SCHEMBL ID69629
MeSH IDM0281224

Synonyms (52)

Synonym
1-bromo-naphthalene
nsc6551
1-naphthyl bromide
.alpha.-bromonaphthalene
90-11-9
naphthalene, 1-bromo-
nsc-6551
1-bromonaphthalene
.alpha.-naphthyl bromide
alpha-naphthyl bromide
alpha-bromonaphthalene
brn 1906414
einecs 201-965-2
nsc 6551
ai3-02271
inchi=1/c10h7br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7
1-bromonaphthalene, 97%
B0618
FT-0663807
AKOS000120011
A843449
bromonaphthalene
27497-51-4
naphthalene, bromo-
unii-976y53p08p
976y53p08p ,
FT-0607535
1-bromonaphthalene [mi]
SCHEMBL69629
a-bromonaphthalene
naphthalen-1-yl bromide
a-naphthyl bromide
1-bromo-naphthaline
bromonapthalene
1-bromonaphtalene
1-bromonapthalene
1-bromonaphthaline
STR06472
mfcd00003868
F9995-1655
1-bromonaphthalene, for synthesis, 97.0%
BBL104373
DTXSID30861681
3,4-diamino-4?-fluorobenzophenone
Q21050994
AMY25810
STL199165
1-bromonaphthalen
SB66920
1-bromonaphthalene; alpha-bromonaphthalene
CS-0017140
EN300-19782
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (8.33)18.2507
2000's5 (41.67)29.6817
2010's5 (41.67)24.3611
2020's1 (8.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 20.13

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 Index20.13 (24.57)
Research Supply Index2.56 (2.92)
Research Growth Index5.07 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.13)

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%
Other12 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
ethylene glycol
Ethylene Glycol: A colorless, odorless, viscous dihydroxy alcohol. It has a sweet taste, but is poisonous if ingested. Ethylene glycol is the most important glycol commercially available and is manufactured on a large scale in the United States. It is used as an antifreeze and coolant, in hydraulic fluids, and in the manufacture of low-freezing dynamites and resins.. ethanediol : Any diol that is ethane or substituted ethane carrying two hydroxy groups.. ethylene glycol : A 1,2-glycol compound produced via reaction of ethylene oxide with water.		2.0210ethanediol;
glycol		metabolite;
mouse metabolite;
solvent;
toxin
formamide
formimidic acid : A carboximidic acid that is formic acid in which the carbonyl oxygen is replaced by an imino group.. primary carboxamide : A carboxamide resulting from the formal condensation of a carboxylic acid with ammonia; formula RC(=O)NH2.		2.4120carboximidic acid;
formamides;
monocarboxylic acid amide;
one-carbon compound		solvent
glycerol
Moon: The natural satellite of the planet Earth. It includes the lunar cycles or phases, the lunar month, lunar landscapes, geography, and soil.		2.0210alditol;
triol		algal metabolite;
detergent;
Escherichia coli metabolite;
geroprotector;
human metabolite;
mouse metabolite;
osmolyte;
Saccharomyces cerevisiae metabolite;
solvent
trifluoperazine
[no description available]		2.0810N-alkylpiperazine;
N-methylpiperazine;
organofluorine compound;
phenothiazines		antiemetic;
calmodulin antagonist;
dopaminergic antagonist;
EC 1.8.1.12 (trypanothione-disulfide reductase) inhibitor;
EC 5.3.3.5 (cholestenol Delta-isomerase) inhibitor;
phenothiazine antipsychotic drug
methylene iodide
methylene iodide: RN given refers to parent cpd		2.4120
hydroxyethyl methacrylate
hydroxyethyl methacrylate: many of cited refs are for gel which refers to polymeric form of above cpd: POLYHYDROXYETHYL METHACRYLATE. 2-hydroxyethyl methacrylate : An enoate ester that is the monomethacryloyl derivative of ethylene glycol.		2.1510enoate esterallergen;
polymerisation monomer
iodine
[no description available]		2.0210halide anion;
monoatomic iodine		human metabolite
boron nitride
[no description available]		2.1510nitride
bromates
Bromates: Negative ions or salts derived from bromic acid, HBrO3.		2.0810bromine oxoanion;
monovalent inorganic anion
organophosphonates
hydrogenphosphite : A divalent inorganic anion resulting from the removal of a proton from two of the hydroxy groups of phosphorous acid.		2.3110divalent inorganic anion;
phosphite ion
betadex
beta-Cyclodextrins: Cyclic GLUCANS consisting of seven (7) glucopyranose units linked by 1,4-glycosidic bonds.		2.7330cyclodextrin
piperidines
Piperidines: A family of hexahydropyridines.		2.0310
ConditionIndicatedRelationship StrengthStudiesTrials