548644
亚氨基芪甲酰氯
90%
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关于此项目
经验公式（希尔记法）:
C15H10ClNO
化学文摘社编号:
分子量:
255.70
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
90%
InChI
1S/C15H10ClNO/c16-15(18)17-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)17/h1-10H
SMILES string
ClC(=O)N1c2ccccc2C=Cc3ccccc13
InChI key
APJYHXJGXDPGBA-UHFFFAOYSA-N
assay
90%
mp
149-153 °C (lit.)
functional group
chloro
Quality Level
General description
Dibenz [b,f]azepine-5-carbonyl chloride or 5H-dibenz [b,f]azepine-5-carbonyl chloride is a tricyclic heterocyclic compound that can be synthesized from 5H-dibenz[ b,f]azepine.
Application
Dibenz [b,f]azepine-5-carbonyl chloride may be used in the preparation of trans-10,11-dibromo-10,11-dihydro-5H-dibenz[b,f]azepine-5-carbonyl chloride via bromination using bromine. It may also be used to prepare urea derivatives, which are potent P2X4 receptor (purinergic receptor) antagonists.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Kinetic evidence for rate determination during the nucleophilic step of olefin bromination. The case of 5H-dibenz [b, f] azepine-5-carbonyl chloride.
Bellucci G and Chiappe C.
The Journal of Organic Chemistry, 58(25), 7120-7127 (1993)
Maoqun Tian et al.
Bioorganic & medicinal chemistry, 22(3), 1077-1088 (2014-01-15)
Antagonists for the P2 receptor subtype P2X4, an ATP-activated cation channel receptor, have potential as novel drugs for the treatment of neuropathic pain and other inflammatory diseases. In the present study, a series of 47 carbamazepine derivatives including 32 novel
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