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Merck

D147206

Sigma-Aldrich

5,6-二甲基苯并咪唑

≥99%

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About This Item

经验公式(希尔记法):
C9H10N2
CAS号:
分子量:
146.19
Beilstein:
116595
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
eCl@ss:
32151902
PubChem物質ID:
NACRES:
NA.22
价格与库存信息目前不能提供

品質等級

化驗

≥99%

形狀

powder

mp

202-205 °C (lit.)

SMILES 字串

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 密鑰

LJUQGASMPRMWIW-UHFFFAOYSA-N

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儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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其他客户在看

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
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
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)
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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