187313
2-Naphthalenemethanol
98%
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About This Item
Formule linéaire :
C10H7CH2OH
Numéro CAS:
Poids moléculaire :
158.20
Numéro MDL:
Code UNSPSC :
12352100
eCl@ss :
39020101
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
98%
Forme
powder
Pf
79-81 °C (lit.)
Groupe fonctionnel
hydroxyl
Chaîne SMILES
OCc1ccc2ccccc2c1
InChI
1S/C11H10O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7,12H,8H2
Clé InChI
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.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Les clients ont également consulté
Anton Kulikov et al.
The Journal of organic chemistry, 73(19), 7611-7615 (2008-09-11)
Irradiation of alcohols, phenols, and carboxylic acids "caged" with the (3-hydroxy-2-naphthalenyl)methyl group results in fast (k(release) approximately = 10(5) s(-1)) release of the substrates with good quantum (Phi = 0.17-0.26) and chemical (>90%) yields. The initial byproduct of the photoreaction
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
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.
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)
Fanyu Zhang et al.
Nature communications, 11(1), 1431-1431 (2020-03-20)
The production of 2D metal-organic frameworks (MOFs) with highly exposed active surfaces is of great importance for catalysis. Here we demonstrate the formation of MOF nanosheets by utilizing CO2 as a capping agent to control the oriented growth of MOF. This
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