Compounds > benzenesulfinic acid
Page last updated: 2024-11-05

benzenesulfinic acid

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

Benzenesulfinic acid is a sulfur-containing organic compound with the formula C6H5SO2H. It is a colorless solid that is soluble in water and ethanol. Benzenesulfinic acid is an important intermediate in the synthesis of other sulfur-containing compounds, such as sulfoxides and sulfones. It is also used as a reducing agent and a catalyst. Benzenesulfinic acid is synthesized by the reaction of benzene with sulfur dioxide in the presence of a catalyst. It is a useful reagent in organic synthesis and is used to prepare various sulfur-containing compounds. Benzenesulfinic acid is a versatile compound with a wide range of applications in organic chemistry and industry. It is studied for its potential applications in pharmaceuticals, pesticides, and other industrial chemicals. Benzenesulfinic acid is a useful reagent for the synthesis of various sulfur-containing compounds and has potential applications in a variety of fields.'

Cross-References

ID SourceID
PubMed CID12057
CHEBI ID32404
SCHEMBL ID9175
SCHEMBL ID16674608
MeSH IDM0386372

Synonyms (30)

Synonym
g9560d97pi ,
nsc 227915
unii-g9560d97pi
einecs 210-548-4
benzenesulfinic-acid-
wln: qso&r
nsc-227915
CHEBI:32404
benzenesulfinic acid
phenylsulfinic acid
nsc227915
618-41-7
benzenesulphinic acid
benzenesulphenic acid
DB03848
AKOS006271434
benzene sulfinic acid
phso2h
SCHEMBL9175
benzenesulfinicacid
sam-760 metabolite 1
DTXSID90210797
J-519682
SCHEMBL16674608
D70177
DS-6058
mfcd00800458
Q7181442
A868622
CS-0156053
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
organosulfinic acidOrganic derivatives of sulfinic acid in which the sulfino group is linked directly to carbon.
[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]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (50.00)29.6817
2010's4 (50.00)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: 31.07

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 Index31.07 (24.57)
Research Supply Index2.40 (2.92)
Research Growth Index4.51 (4.65)
Search Engine Demand Index32.31 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.07)

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%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
gallic acid
gallate : A trihydroxybenzoate that is the conjugate base of gallic acid.		2.2110trihydroxybenzoic acidantineoplastic agent;
antioxidant;
apoptosis inducer;
astringent;
cyclooxygenase 2 inhibitor;
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor;
geroprotector;
human xenobiotic metabolite;
plant metabolite
divinyl sulfone
divinyl sulfone: cross-linking reagent for agarose gels. divinyl sulfone : A sulfone compound having two S-vinyl substituents.		2.0610sulfonecross-linking reagent
n-butyl mercaptan
n-butyl mercaptan: hydrolytic product of merphos; RN given refers to parent cpd		210alkanethiol
piperidine
[no description available]		2.0310azacycloalkane;
piperidines;
saturated organic heteromonocyclic parent;
secondary amine		base;
catalyst;
human metabolite;
non-polar solvent;
plant metabolite;
protic solvent;
reagent
palladium
Palladium: A chemical element having an atomic weight of 106.4, atomic number of 46, and the symbol Pd. It is a white, ductile metal resembling platinum, and following it in abundance and importance of applications. It is used in dentistry in the form of gold, silver, and copper alloys.. palladium : Chemical element (nickel group element atom) with atomic number 46.		7.4520metal allergen;
nickel group element atom;
platinum group metal atom
silver
Silver: An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.		210copper group element atom;
elemental silver		Escherichia coli metabolite
rhamnose
[no description available]		2.0310L-rhamnose
alkenes
[no description available]		2.4620
trifluoromethanesulfonic acid
trifluoromethanesulfonic acid: deblocking reagent for peptide synthesis; RN given refers to parent cpd. triflic acid : A one-carbon compound that is methanesulfonic acid in which the hydrogens attached to the methyl carbon have been replaced by fluorines.		2.4220one-carbon compound;
perfluoroalkanesulfonic acid
1,2-bis(phenylsulfonyl)ethane
[no description available]		7.0610
glycero-manno-heptose
glycero-manno-heptose: N1 same as NM; RN given refers to (L-glycero-D-manno)-isomer		2.0310
2-oxindole
2-oxindole: RN given refers to parent cpd; structure. indolin-2-one : An indolinone carrying an oxo group at position 2.		2.110gamma-lactam;
indolinone
glycosides
[no description available]		210
piperidines
Piperidines: A family of hexahydropyridines.		2.4220
ConditionIndicatedRelationship StrengthStudiesTrials