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Sigma-Aldrich

9-Methyladenine

97%

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About This Item

Fórmula empírica (notación de Hill):
C6H7N5
Número de CAS:
700-00-5
Peso molecular:
149.15
MDL number:
MFCD00047232
UNSPSC Code:
12352100
PubChem Substance ID:
24878931
NACRES:
NA.22

assay

97%

mp

300-305 °C (lit.)

SMILES string

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)

InChI key

WRXCXOUDSPTXNX-UHFFFAOYSA-N

Gene Information

rat ... Adora1(29290) , Adora2a(25369)

Categorías relacionadas

General description

9-Methyladenine is a derivative of adenine. It belongs to the monoclinic crystal system and P21/c space group.

Application

9-Methyladenine may be used in the preparation of N6-benzoyl-9-methyladenine.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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)
Susana Ibáñez et al.
Inorganic chemistry, 50(20), 10439-10447 (2011-09-24)
The synthesis and characterization of three heteronuclear Pt(2)Pd(2) (4, 5) and PtPd(2) (6) complexes of the model nucleobase 9-methyladenine (9-MeA) is reported. The compounds were prepared by reacting [Pt(NH(3))(3)(9-MeA-N7)](ClO(4))(2) (1) with [Pd(en)(H(2)O)(2)](ClO(4))(2) at different ratios r between Pt and Pd
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
Diego Montagner et al.
Inorganic chemistry, 49(5), 2103-2110 (2010-02-09)
Deprotonation of 1-methylcytosine (1-MeCy) and 9-methyladenine (9-MeAd) promoted by cis-[L(2)Pt(mu-OH)](2)(NO(3))(2) (L = PPh(3), PMePh(2), (1)/(2)dppe) in PhCN causes the irreversible insertion of a nitrile molecule into the Pt-N4 and Pt-N6 bonds of the cytosinate and adeninate ligands, respectively, to form
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