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548644

Sigma-Aldrich

Dibenz [b,f]azepine-5-carbonyl chloride

90%

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About This Item

Empirical Formula (Hill Notation):
C15H10ClNO
CAS Number:
33948-22-0
Molecular Weight:
255.70
MDL number:
MFCD00792462
UNSPSC Code:
12352100
PubChem Substance ID:
24879048
NACRES:
NA.22

Quality Level

200

Assay

90%

mp

149-153 °C (lit.)

functional group

chloro

SMILES string

ClC(=O)N1c2ccccc2C=Cc3ccccc13

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

InChI key

APJYHXJGXDPGBA-UHFFFAOYSA-N

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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.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

548644-BULK:
548644-5G:
548644-VAR:
548644-25G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ2213
MKCL3896
MKCJ7993
MKCG8865
MKBW5960V

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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
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)

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