83600
Resorcinol
puriss., ≥99.0% (HPLC)
Synonym(s):
1,3-Benzenediol
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About This Item
Linear Formula:
C6H4-1,3-(OH)2
CAS Number:
Molecular Weight:
110.11
EC Number:
203-585-2
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
906905
InChI
1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H
InChI key
GHMLBKRAJCXXBS-UHFFFAOYSA-N
SMILES string
Oc1cccc(O)c1
vapor density
3.8 (vs air)
vapor pressure
1 mmHg ( 21.1 °C)
grade
puriss.
assay
≥99.0% (HPLC)
autoignition temp.
1126 °F
mp
109-111 °C
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may discolor on storage
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Andriy I Vovk et al.
Bioorganic & medicinal chemistry letters, 19(5), 1314-1317 (2009-02-12)
Resorcinarene oxazines bearing four TEMPO fragments at the wide rim of the macrocycle were prepared through the aminomethylation of resorcinarene octols with 4-amino-TEMPO and formaldehyde. Tetra-TEMPO resorcinarenes are efficient scavengers of 1,1-diphenyl-2-picrylhydrazyl radicals. The model studies revealed that macrocyclic structure
Graziella Tocco et al.
Bioorganic & medicinal chemistry letters, 19(1), 36-39 (2008-12-05)
In this work, the PEG-immobilization and the liquid phase synthesis of some coumarins derived from cardol are presented. Some preliminary results on their tyrosinase inhibitory activity are also included.
S L da Silva et al.
European journal of medicinal chemistry, 44(1), 312-321 (2008-04-22)
Phospholipases A(2) are enzymes responsible for the hydrolysis of membrane phospholipids that release arachidonic acid, which serves as substrate for pro-inflammatory mediators, such as prostaglandins and leucotriens. The design of specific inhibitors for PLA(2) might help in the development of
Giovanni Appendino et al.
Journal of natural products, 71(8), 1427-1430 (2008-08-07)
Marijuana (Cannabis sativa) has long been known to contain antibacterial cannabinoids, whose potential to address antibiotic resistance has not yet been investigated. All five major cannabinoids (cannabidiol (1b), cannabichromene (2), cannabigerol (3b), Delta (9)-tetrahydrocannabinol (4b), and cannabinol (5)) showed potent
Alessio Innocenti et al.
Bioorganic & medicinal chemistry, 16(15), 7424-7428 (2008-06-27)
Inhibition of 12 mammalian isoforms of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), CA I-XIV, with a series of phenols was investigated. The inhibition profile by phenols of these CAs was distinct from those of the sulfonamides and their isosteres
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