515108
5-Methoxybenzimidazole
97%
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About This Item
Empirical Formula (Hill Notation):
C8H8N2O
CAS Number:
Molecular Weight:
148.16
PubChem Substance ID:
eCl@ss:
32151902
UNSPSC Code:
12352100
NACRES:
NA.22
EC Number:
225-502-9
MDL number:
InChI key
ILMHAGCURJPNRZ-UHFFFAOYSA-N
InChI
1S/C8H8N2O/c1-11-6-2-3-7-8(4-6)10-5-9-7/h2-5H,1H3,(H,9,10)
SMILES string
COc1ccc2[nH]cnc2c1
assay
97%
mp
121-126 °C (lit.)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Kristi Kincaid et al.
Nucleic acids research, 33(8), 2620-2628 (2005-05-10)
In order to further understand how DNA polymerases discriminate against incorrect dNTPs, we synthesized two sets of dNTP analogues and tested them as substrates for DNA polymerase alpha (pol alpha) and Klenow fragment (exo-) of DNA polymerase I (Escherichia coli).
Computational determination of aqueous p K a values of protonated benzimidazoles (Part 2).
Brown TN and Mora-Diez N.
The Journal of Physical Chemistry B, 110(41), 20546-20554 (2006)
Structural investigation of the biosynthesis of alternative lower ligands for cobamides by nicotinate mononucleotide: 5, 6-dimethylbenzimidazole phosphoribosyltransferase from Salmonella enterica.
Cheong C, et al.
The Journal of Biological Chemistry, 276(40), 37612-37620 (2001)
On the Biosynthesis of 5-Methoxybenzimidazole.
Wurm R, et al.
European Journal of Biochemistry, 56(2), 427-432 (1975)
An exceptionally mild catalytic thioester aldol reaction inspired by polyketide biosynthesis.
Lalic G, et al.
Journal of the American Chemical Society, 125(10), 2852-2853 (2003)
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