389439
1-Pyrenemethanol
98%
Sinonimo/i:
1-(1-Hydroxymethyl)pyrene, 1-Hydroxymethylpyrene
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About This Item
Formula empirica (notazione di Hill):
C17H12O
Numero CAS:
Peso molecolare:
232.28
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
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Livello qualitativo
Saggio
98%
Stato
solid
Punto di fusione
123-126 °C (lit.)
Gruppo funzionale
hydroxyl
Stringa SMILE
OCc1ccc2ccc3cccc4ccc1c2c34
InChI
1S/C17H12O/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12/h1-9,18H,10H2
NGDMLQSGYUCLDC-UHFFFAOYSA-N
Applicazioni
1-Pyrenemethanol can be used:
- For the synthesis of pincer-like benzene-bridged fluorescent selective sensor for adenosine-5′-triphosphate (ATP) detection.
- As a starting material for the synthesis of pyrene-end poly(glycidyl methacrylate) polymer.
- As an initiator for the synthesis of pyrene core star polymers.
- For the synthesis of 1-pyrenecarboxaldehyde, an important intermediate in pharmaceutical and agrochemical fields.
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)
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I clienti hanno visto anche
H Glatt et al.
Carcinogenesis, 14(4), 599-602 (1993-04-01)
1-Hydroxymethylpyrene (HMP), a primary benzylic alcohol, and 4H-cyclopenta[def]chrysen-4-ol (OH-CPC), a secondary benzylic alcohol, were investigated for mutagenicity in Salmonella typhimurium (reversion of the his- strain TA98) in the presence of various xenobiotic-metabolizing systems. In the direct test, HMP was inactive
Encapsulation of functional moieties within branched star polymers: effect of chain length and solvent on site isolation.
Hecht S, et al.
Journal of the American Chemical Society, 123(1), 18-25 (2001)
Walter Meinl et al.
Pharmacogenetics, 12(9), 677-689 (2002-12-05)
Various enzymatically formed sulfuric acid esters are chemically reactive and mutagenic. This metabolic activation pathway is not detected in standard in-vitro mutagenicity test systems. We describe the construction of Salmonella typhimurium TA1538-derived strains expressing alloenzymes *1, *2, *3, *5, *6
Highly efficient oxidation of alcohols to carbonyl compounds in the presence of molecular oxygen using a novel heterogeneous ruthenium catalyst.
Ji H, et al.
Tetrahedron Letters, 43(40), 7179-7183 (2002)
H Glatt et al.
Chemico-biological interactions, 109(1-3), 195-219 (1998-05-05)
Sulfation is a common final step in the biotransformation of xenobiotics and is traditionally associated with inactivation. However, the sulfate group is electron-withdrawing and may be cleaved off heterolytically in some molecules leading to electrophilic cations which may form adducts
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 389439-10G | 4061831970791 |
| 389439-1G | 4061831970852 |
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