M29800
2-甲基苯并咪唑
98%
别名:
2-甲基-1H-1,3-苯并二唑, 2-甲基-1H-苯并[d]咪唑, 2-甲基-1H-苯并咪唑, 2-甲基苯并咪唑
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关于此项目
经验公式（希尔记法）:
C8H8N2
化学文摘社编号:
分子量:
132.16
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32151902
UNSPSC Code:
12352100
EC Number:
210-411-9
MDL number:
Beilstein/REAXYS Number:
112264
产品名称
2-甲基苯并咪唑, 98%
InChI key
LDZYRENCLPUXAX-UHFFFAOYSA-N
InChI
1S/C8H8N2/c1-6-9-7-4-2-3-5-8(7)10-6/h2-5H,1H3,(H,9,10)
SMILES string
Cc1nc2ccccc2[nH]1
assay
98%
mp
175-177 °C (lit.)
Quality Level
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Application
- 2-甲基苯并咪唑是一种重要的药效团，广泛用于药物化学中，可用于合成各种抗菌和抗真菌剂。
- 可用作合成取代的苯并咪唑[1,2-a]喹诺酮类物质的关键前体。
- 它可用于合成可逆的固-液相转变配位聚合物晶体。
- 2-甲基苯并咪唑还表现出腐蚀抑制作用。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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We have recently reported that a series of (E)-8-styrylcaffeines and (E)-2-styrylbenzimidazoles are moderate to very potent competitive inhibitors of monoamine oxidase B (MAO-B). The most potent member of the series was found to be (E)-8-(3-chlorostyryl)caffeine (CSC) with an enzyme-inhibitor dissociation
Synthesis and biological evaluation of substituted benzimidazoles.
Shah K, et al.
Journal of the Indian Chemical Society, 93, 1009-1018 (2016)
Synthesis and Antimicrobial Activity of Some Benzimidazole and 2-Methylbenzimidazole Derivatives.
Jain P and Tiwari M
Asian Journal of Chemistry, 29(4), 838-838 (2017)
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