547328
9-Methyladenine
97%
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About This Item
Fórmula empírica (notación de Hill):
C6H7N5
Número de CAS:
Peso molecular:
149.15
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
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Ensayo
97%
mp
300-305 °C (lit.)
cadena SMILES
Cn1cnc2c(N)ncnc12
InChI
1S/C6H7N5/c1-11-3-10-4-5(7)8-2-9-6(4)11/h2-3H,1H3,(H2,7,8,9)
Clave InChI
WRXCXOUDSPTXNX-UHFFFAOYSA-N
Información sobre el gen
rat ... Adora1(29290) , Adora2a(25369)
Descripción general
9-Methyladenine is a derivative of adenine. It belongs to the monoclinic crystal system and P21/c space group.
Aplicación
9-Methyladenine may be used in the preparation of N6-benzoyl-9-methyladenine.
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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Sulayman A Oladepo et al.
The journal of physical chemistry. B, 115(19), 6149-6156 (2011-04-23)
The photophysics and photochemistry of nucleobases are the factors governing the photostability of DNA and RNA, since they are the UV chromophores in nucleic acids. Because the formation of photoproducts involves structural changes in the excited electronic state, we study
Chris T Middleton et al.
The journal of physical chemistry. A, 111(42), 10460-10467 (2007-10-04)
Vibrational cooling by 9-methyladenine was studied in a series of solvents by femtosecond transient absorption spectroscopy. Signals at UV and near-UV probe wavelengths were assigned to hot ground state population created by ultrafast internal conversion following electronic excitation by a
Excited state spectroscopy and dynamics of isolated adenine and 9-methyladenine.
Luhrs DC, et al.
Physical Chemistry Chemical Physics, 3(10), 1827-1831 (2001)
Szymon Smolarek et al.
Physical chemistry chemical physics : PCCP, 12(48), 15600-15606 (2010-08-03)
High-resolution absorption spectra of adenine, 9-methyladenine and 2-aminopurine in helium nanodroplets have been recorded. In contrast to molecular beam experiments, large variations in linewidths are observed for adenine and 9-methyladenine. At the same time, the spectrum of 2-aminopurine remains sharp
Tomomi Noguchi-Yachide et al.
Bioorganic & medicinal chemistry, 23(5), 953-959 (2015-02-14)
Bromodomain and extra-terminal domain (BET) proteins are epigenetic readers that bind to acetylated lysines in histones. Among them, BRD4 is a candidate target molecule of therapeutic agents for diverse diseases, including cancer and inflammatory disease. As a part of our
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