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83600

Sigma-Aldrich

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:
108-46-3
Molecular Weight:
110.11
Beilstein:
906905
EC Number:
203-585-2
MDL number:
MFCD00002269
UNSPSC Code:
12352100

vapor density

3.8 (vs air)

vapor pressure

1 mmHg ( 21.1 °C)

grade

puriss.

Assay

≥99.0% (HPLC)

autoignition temp.

1126 °F

bp

178 °C/16 mmHg (lit.)

mp

109-111 °C
109-112 °C (lit.)

SMILES string

Oc1cccc(O)c1

InChI

1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H

InChI key

GHMLBKRAJCXXBS-UHFFFAOYSA-N

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Caution

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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