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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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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Chemical communications (Cambridge, England), 47(40), 11249-11251 (2011-09-20)
Immobilisation of vitamin B12 allows synthesising a biomimetic base-off/histidine-on complex that resembles structural features of cobalamin dependent enzyme active sites.
Pseudo-B12 joins the cofactor family.
Journal of bacteriology, 190(4), 1157-1159 (2007-12-18)
Proceedings of the National Academy of Sciences of the United States of America, 104(8), 2921-2926 (2007-02-16)
The synthesis of 5,6-dimethylbenzimidazole (DMB), the lower ligand of coenzyme B(12), has remained elusive. We report in vitro and in vivo evidence that the BluB protein of the photosynthetic bacterium Rhodospirillum rubrum is necessary and sufficient for catalysis of the
Dalton transactions (Cambridge, England : 2003), (3)(3), 424-433 (2009-01-06)
The structure of nitrosylcobalamin (NOCbl) in solution has been studied by NMR spectroscopy and the 1H and 13C NMR spectra have been assigned. 13C and 31P NMR chemical shifts, the UV-vis spectrum of NOCbl and the observed pKbase-off value of
Nature, 446(7134), 449-453 (2007-03-23)
Vitamin B12 (cobalamin) is among the largest known non-polymeric natural products, and the only vitamin synthesized exclusively by microorganisms. The biosynthesis of the lower ligand of vitamin B(12), 5,6-dimethylbenzimidazole (DMB), is poorly understood. Recently, we discovered that a Sinorhizobium meliloti
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