592277
2-氯苯并咪唑
98%
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关于此项目
经验公式（希尔记法）:
C7H5ClN2
化学文摘社编号:
分子量:
152.58
PubChem Substance ID:
eCl@ss:
32151902
UNSPSC Code:
12352100
NACRES:
NA.22
EC Number:
225-453-3
MDL number:
产品名称
2-氯苯并咪唑, 98%
InChI key
AYPSHJCKSDNETA-UHFFFAOYSA-N
InChI
1S/C7H5ClN2/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H,9,10)
SMILES string
Clc1nc2ccccc2[nH]1
assay
98%
form
solid
mp
207-211 °C (lit.)
functional group
chloro
Quality Level
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Application
2-Chlorobenzimidazole can be used to synthesize the following:
- 1-methyl-2-chlorobenzimidazole via reaction with dimethyl sulfate
- 1-ethyl-2-chlorobenzimidazole via reaction with diethyl sulfate
- 1-benzyl-2-chlorobenzimidazole via reaction with benzyl chloride
- 2-chloro-4,5,6,7-tetrabromobenzimidazole via bromination with bromine
General description
2-Chlorobenzimidazole can be synthesized by reacting benzimidazole-2-one with phosphoryl chloride in the presence of phenol.
signalword
Warning
hcodes
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
法规信息
新产品
此项目有
?A facile and green synthesis of N-substituted-2-chlorobenzimidazoles?
Rao S.S, et al.
Der Pharma Chemica, 5(06), 69- 72 (2013)
?Polyhalogenobenzimidazoles: Synthesis and Their InhibitoryActivity against Casein Kinases?
Andrzejewska M, et al.
Bioorganic & Medicinal Chemistry, 11(18), 3997- 4002 (2003)
?Discovery of pyrimidine benzimidazoles as Src-family selective Lck inhibitors. Part II?
Zhang G, et al.
Bioorganic & Medicinal Chemistry, 19(23), 6691-6695 (2009)
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