Passa al contenuto
Merck
Tutte le immagini(3)

Documenti

187313

Sigma-Aldrich

2-Naphthalenemethanol

98%

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(3)

About This Item

Formula condensata:
C10H7CH2OH
Numero CAS:
1592-38-7
Peso molecolare:
158.20
Numero MDL:
MFCD00004124
Codice UNSPSC:
12352100
eCl@ss:
39020101
ID PubChem:
24851267
NACRES:
NA.22

Saggio

98%

Forma fisica

powder

Punto di fusione

79-81 °C (lit.)

Stringa SMILE

OCc1ccc2ccccc2c1

InChI

1S/C11H10O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7,12H,8H2
MFGWMAAZYZSWMY-UHFFFAOYSA-N

Applicazioni

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.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 5

1 of 5

1-Pyrenemethyl methacrylate contains ≤200 ppm MEHQ as inhibitor, 99% (GC)

Sigma-Aldrich

765120

1-Pyrenemethyl methacrylate

4-Methylbenzyl alcohol 98%

Sigma-Aldrich

127809

4-Methylbenzyl alcohol

1-Naphthaldehyde 95%

Sigma-Aldrich

N109

1-Naphthaldehyde

2-Thiophenemethanol 98%

Sigma-Aldrich

T32654

2-Thiophenemethanol

2-Methylnaphthalene (β) 95%

Sigma-Aldrich

M57006

2-Methylnaphthalene (β)

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

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.