250937
1,6-Dimethylnaphthalene
99%
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
About This Item
Formula condensata:
C10H6(CH3)2
Numero CAS:
Peso molecolare:
156.22
Beilstein:
1854429
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
99%
Indice di rifrazione
n20/D 1.606 (lit.)
P. eboll.
265-266 °C (lit.)
Punto di fusione
−17-−16 °C (lit.)
Densità
1.002 g/mL at 25 °C (lit.)
Stringa SMILE
Cc1ccc2c(C)cccc2c1
InChI
1S/C12H12/c1-9-6-7-12-10(2)4-3-5-11(12)8-9/h3-8H,1-2H3
CBMXCNPQDUJNHT-UHFFFAOYSA-N
Informazioni sul gene
human ... CYP1A2(1544)
Cerchi prodotti simili? Visita Guida al confronto tra prodotti
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
233.6 °F - closed cup
Punto d’infiammabilità (°C)
112 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
Loaded liquid scintillators based on 1, 6-dimethylnaphthalene and 1-methylnaphthalene.
Koike Y and Yamamoto K.
Nuclear Instruments and Methods in Physics Research, 84(1), 24-28 (1970)
The assessment of some volatile organic compounds as sprout suppressants for ware and seed potatoes.
Beveridge JL, et al.
Potato Research, 24(1), 61-76 (1981)
Nien-Hsin Kao et al.
Marine pollution bulletin, 97(1-2), 319-332 (2015-06-08)
Three fishing harbors were investigated to study the polycyclic aromatic hydrocarbons in the sediments and trace possible anthropogenic sources by identification of cyclic terpenoid biomarkers. Seventeen terpanes, 10 steranes and 10 bicyclic sesquiterpanes in the marine diesel and the three
Kunal Roy et al.
European journal of medicinal chemistry, 44(5), 1941-1951 (2008-12-27)
A series of naphthalene and non-naphthalene derivatives (n=42) having cytochrome P450 2A6 and 2A5 inhibitory activities, reported by Rahnasto et al., were subjected to QSAR and QAAR studies. The analyses were performed using electronic, spatial, shape and thermodynamic descriptors to
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the
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.