187313
2-Naphthalenemethanol
98%
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About This Item
Linear Formula:
C10H7CH2OH
CAS Number:
Molecular Weight:
158.20
UNSPSC Code:
12352100
eCl@ss:
39020101
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Assay:
98%
Form:
powder
Quality Level
assay
98%
form
powder
mp
79-81 °C (lit.)
functional group
hydroxyl
SMILES string
OCc1ccc2ccccc2c1
InChI
1S/C11H10O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7,12H,8H2
InChI key
MFGWMAAZYZSWMY-UHFFFAOYSA-N
Application
2-Naphthalenemethanol was used as marker in the determination of critical micelle concentration of anionic surfactants by capillary electrophoresis. It was used in the synthesis of acetate protected xylosides.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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T P Binder et al.
Molecular pharmacology, 33(4), 477-479 (1988-04-01)
Aryl sulfotransferase (AST) IV catalyzes the 3'-phosphoadenosine 5'-phosphosulfate-dependent sulfation of a variety of benzylic alcohols. Several molecular characteristics of benzylic alcohols were investigated for their ability to influence the catalytic efficiency of a homogeneous preparation of rat hepatic AST IV.
Karin Holmqvist et al.
Bioorganic & medicinal chemistry, 21(11), 3310-3317 (2013-04-23)
Proteoglycans (PGs) are important macromolecules in mammalian cells, consisting of a core protein substituted with carbohydrate chains, known as glycosaminoglycans (GAGs). Simple xylosides carrying hydrophobic aglycons can enter cells and act as primers for GAG chain synthesis, independent of the
Determination of critical micelle concentration of anionic surfactants by capillary electrophoresis using 2-naphthalenemethanol as a marker for micelle formation.
Nakamura H, et al.
Analytical Sciences, 14(2), 379-382 (1998)