D110000
3,5-Dihydroxybenzoic acid
97%
Sinónimos:
α-Resorcylic acid
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Fórmula lineal:
(HO)2C6H3CO2H
Número CAS:
Peso molecular:
154.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-730-7
Beilstein/REAXYS Number:
2207864
MDL number:
Assay:
97%
Form:
powder
Servicio técnico
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97%
form
powder
mp
236-238 °C (dec.) (lit.)
SMILES string
OC(=O)c1cc(O)cc(O)c1
InChI
1S/C7H6O4/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,8-9H,(H,10,11)
InChI key
UYEMGAFJOZZIFP-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Clase de almacenamiento
11 - Combustible Solids
flash_point_f
392.0 °F - closed cup
flash_point_c
200 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Seetharaman Vaidyanathan et al.
Rapid communications in mass spectrometry : RCM, 20(8), 1192-1198 (2006-03-17)
Matrix-assisted laser desorption/ionisation (MALDI) mass spectrometry was investigated for the simultaneous detection of several metabolites, as applicable to global metabolite analysis (metabolomics). The commonly employed organic matrices alpha-cyano-4-hydroxycinnamic acid and 3,5-dihydroxybenzoic acid, in both the crystalline and ionic liquid forms
Silke C Wenzel et al.
Chembiochem : a European journal of chemical biology, 9(16), 2711-2721 (2008-10-31)
Kendomycin is a bioactive polyketide that is produced by various Streptomyces strains. It displays strong antibiotic activities against a wide range of bacteria and exhibits remarkable cytotoxic effects on the growth of several human cancer cell lines. In this study
Abigail E Wolfe et al.
Biochemistry, 46(19), 5741-5753 (2007-04-21)
Dihydroorotate dehydrogenases (DHODs) catalyze the oxidation of dihydroorotate to orotate in the only redox reaction in pyrimidine biosynthesis. The pyrimidine binding sites are very similar in all structurally characterized DHODs, suggesting that the prospects for identifying a class-specific inhibitor directed