41350
2,6-Dimethylphenol
purum, ≥98.0% (GC)
Synonym(s):
2-Hydroxy-m-xylene, vic.-m-Xylenol
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About This Item
Linear Formula:
(CH3)2C6H3OH
CAS Number:
Molecular Weight:
122.16
EC Number:
209-400-1
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1446677
grade
purum
assay
≥98.0% (GC)
autoignition temp.
1110 °F
bp
203 °C (lit.)
mp
43-45 °C (lit.), 43-48 °C
SMILES string
Cc1cccc(C)c1O
InChI
1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3
InChI key
NXXYKOUNUYWIHA-UHFFFAOYSA-N
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Murat Sentürk et al.
Bioorganic & medicinal chemistry, 17(8), 3207-3211 (2009-02-24)
The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I and II, with a series of phenol derivatives was investigated by using the esterase assay, with 4-nitrophenyl acetate as substrate. 2,6-Dimethylphenol, 2,6-diisopropylphenol (propofol), 2,6-di-t-butylphenol, butylated hydroxytoluene, butylated
Jerry O Ebalunode et al.
Bioorganic & medicinal chemistry, 17(14), 5133-5138 (2009-06-13)
Current anesthetics, especially the inhaled ones, have troublesome side effects and may be associated with durable changes in cognition. It is therefore highly desirable to develop novel chemical entities that reduce these effects while preserving or enhancing anesthetic potency. In
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following