D147206
5,6-Dimethylbenzimidazole
≥99%
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About This Item
Fórmula empírica (notación de Hill):
C9H10N2
Número de CAS:
Peso molecular:
146.19
Beilstein/REAXYS Number:
116595
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
32151902
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
≥99%
form
powder
mp
202-205 °C (lit.)
SMILES string
Cc1cc2nc[nH]c2cc1C
InChI
1S/C9H10N2/c1-6-3-8-9(4-7(6)2)11-5-10-8/h3-5H,1-2H3,(H,10,11)
InChI key
LJUQGASMPRMWIW-UHFFFAOYSA-N
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Categorías relacionadas
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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Los clientes también vieron
Peter J Anderson et al.
Journal of bacteriology, 190(4), 1160-1171 (2007-11-06)
Corrinoid (vitamin B12-like) cofactors contain various alpha-axial ligands, including 5,6-dimethylbenzimidazole (DMB) or adenine. The bacterium Salmonella enterica produces the corrin ring only under anaerobic conditions, but it can form "complete" corrinoids aerobically by importing an "incomplete" corrinoid, such as cobinamide
Ruibing Wang et al.
Dalton transactions (Cambridge, England : 2003), (18)(18), 3584-3589 (2009-04-22)
Cucurbit[7]uril (CB[7]) forms very stable complexes with the alpha-axial 5,6-dimethylbenzimidazole (alpha-DMB) nucleotide base when dissociated from the Co(III) center in vitamin B(12) (CNCbl, K(CB[7]) = (7.5 +/- 0.5) x 10(4) dm(3) mol(-1)) and coenzyme B(12) (AdoCbl, K(CB[7]) = (3.02 +/-
Biochemistry: molecular cannibalism.
Steven E Ealick et al.
Nature, 446(7134), 387-388 (2007-03-23)
Xiao-Lei Wang et al.
Journal of the American Chemical Society, 133(11), 4079-4091 (2011-02-25)
BluB is a distinct flavin destructase that catalyzes a complex oxygen-dependent conversion of reduced flavin mononucleotide (FMNH(2)) to form 5,6-dimethylbenzimidazole (DMB), the lower ligand of vitamin B(12). The catalyzed mechanism remains a challenge due to the discrepancy between the complexity
V Krishnakumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 811-816 (2007-05-04)
The vibrational spectra of 5,6-dimethyl benzimidazole (5,6DBZ) have been computed using the standard B3LYP/6-311G** method and basis set combinations. The solid phase FT-IR and FT-Raman spectra were recorded in the region 4000-400 and 3500-100 cm(-1), respectively. A close agreement was
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