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Substance
ID:1822722
Structure
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Functional Group
Text
ID:89764
3-hydroxybenzoic acid
Chemical Entities of Biological Interest
ID: CHEBI:30764
Names and Identifiers
IUPAC name
3-hydroxybenzoic acid
IUPAC Traditional name
3-hydroxybenzoic acid
Synonyms
3-hydroxybenzoic acid
3-HYDROXYBENZOIC ACID
3-Hydroxybenzoic acid
3-carboxyphenol
m-Hydroxybenzoic acid
m-hydroxybenzoic acid
m-salicylic acid
Registration numbers
CAS Number
99-06-9
Wikipedia Title
3-Hydroxybenzoic_acid
PubChem CID
7420
Beilstein Number
508160
KEGG ID
C00587
KNApSAcK Database
C00040822
PubMed Citation Links
23718125
23113660
23392766
21539432
28166217
Reaxys Registry
508160
ACToR Database
99-06-9
10476-50-3
BKMS React Database
13194
1002
3970
210
BRENDA Database
2.3.1.133
1.14.13.24
1.10.3.1
4.1.1.46
4.1.1.55
4.2.1.1
3.1.1.20
1.1.1.24
1.14.13.2
1.4.3.3
1.14.13.35
1.14.13.33
1.14.11.2
1.13.11.8
1.13.11.3
1.11.1.11
2.4.1.194
1.13.11.33
1.14.13.23
6.2.1.37
6.3.2.14
6.2.1.71
6.2.1.74
1.2.99.6
6.2.1.25
2.4.1.177
4.1.3.45
1.14.99.23
2.1.1.274
3.1.6.1
3.5.5.1
1.2.1.24
1.2.1.64
1.2.1.7
1.2.1.28
1.2.3.9
1.2.1.5
1.2.3.8
1.3.1.28
1.14.99.15
3.1.1.1
3.4.21.19
1.2.3.1
1.17.3.2
1.2.1.3
1.2.1.16
1.2.1.67
1.2.1.65
3.1.2.20
1.14.14.1
3.4.16.4
1.2.99.7
1.2.1.30
1.14.14.92
2.1.1.273
2.7.7.97
1.14.13.7
6.2.1.62
1.13.11.4
BRENDA Ligand Database
3970
1002
13194
210
CHEMBL
CHEMBL65369
CompTox Database
DTXSID6021610
MetaboLights Database
MTBLS4722
MTBLS4967
MTBLS530
MTBLS461
MTBLS615
MTBLS4012
MTBLS926
MTBLS1115
MTBLS1182
MTBLS2406
MTBLS1411
MTBLS138
MTBLS1561
MTBLS298
MTBLS3003
MTBLS3518
MTBLS3657
MTBLS406
MTBLS3935
MTBLS4099
MTBLS2105
MTBLS1906
MTBLS1903
MTBLS2224
Protein Data Bank
3tus
2dkh
3pcb
3sa4
4bk1
4pai
4q6w
5a3k
5hpi
5i7i
6o9a
6sj3
7trw
SABIO-RK Database
6705
6707
2495
12394
6943
12737
13784
7702
SureChEMBL Database
SCHEMBL40078
UniProt Database
Q6XMI3
O22822
Q66PF4
Q9AJS8
Q9F131
Q0QFQ1
Q8NLB6
Q5EXK1
Q3S4B7
P77589
Q8NLB7
HMDB Database
HMDB0002466
PDBeChem Database
3HB
Golm Database
6673358f-9598-40c9-aecc-38d824491b9b
f7c0eb19-623b-460c-9d60-58af3b402d9e
85dc57e7-fcd9-4ec1-92c0-d2d39106fc62
74d73f28-845f-449f-8a7b-e4791b7e51eb
5c530ad7-0b97-4c30-bf04-eb604931d319
NMRShiftDB Database
10024829
Patent number
US2008193377
EP1754705
US2007010579
US2007178123
BindingDB Database
50336491
Gmelin ID
3338
CHEBI ID
CHEBI:30764
CHEBI:1538
CHEBI:39892
CHEBI:20064
PubChem SID
8145232
Properties
No Data Available
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Molecule Details
A monohydroxybenzoic acid that is benzoic acid substituted by a hydroxy group at position 3. It has been isolated from Taxus baccata. It is used as an intermediate in the synthesis of plasticisers, resins, pharmaceuticals, etc.
Molecular Spectra
No Data Available
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References
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