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Merck
CN

515108

5-甲氧基苯并咪唑

97%

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关于此项目

经验公式(希尔记法):
C8H8N2O
化学文摘社编号:
分子量:
148.16
PubChem Substance ID:
eCl@ss:
32151902
UNSPSC Code:
12352100
NACRES:
NA.22
EC Number:
225-502-9
MDL number:
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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.)

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
On the Biosynthesis of 5-Methoxybenzimidazole.
Wurm R, et al.
European Journal of Biochemistry, 56(2), 427-432 (1975)
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)
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).
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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