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5H-Dibenz[b,f]azepine

ALDRICH/143650 - 97%

Synonym: Iminostilbene

CAS Number: 256-96-2
Empirical Formula (Hill Notation): C14H11N
Molecular Weight: 193.24
EC Number: 205-970-0
MDL Number: MFCD00005071
Linear Formula: C14H11N
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-143650-1G 1 g
 $0.00
1/EA
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45-143650-5G 5 g
 $129.00
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assay 97%
InChI 1S/C14H11N/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)15-13/h1-10,15H
InChI key LCGTWRLJTMHIQZ-UHFFFAOYSA-N
mp 196-199 °C (lit.)
Quality Level 200 
SMILES string N1c2ccccc2C=Cc3ccccc13
solubility ethyl acetate: soluble 25 mg/mL, clear, yellow to orange
Application: 5H-Dibenz[b,f]azepine can be used:
• As a starting material to prepare pharmacologically important dibenzoazepine-pyridazine derivatives.
• To synthesize 3-chloro-1-(5H-dibenz[b,f]azepine-5yl)propan-1-one, a key intermediate used to prepare aminophenol derivatives.
• In the synthesis of dibenzazepine derivatives.
• As a starting material to synthesize olefinic multidentate ligand, which is used to prepare Rh(I) complexes.
Biochem/physiol Actions: 2-(Bromomethyl)naphthalene is a fluorescent alkyl bromide. It causes the esterification of free carboxyl groups formed at the surface of polyethylene terephthalate by enzyme hydrolysis. It acts as organic electrophile in the P4S10/acyloin reaction.
General description: 5H-Dibenz[b,f]azepine, a tricyclic amine with a seven-membered ring, is commonly known as iminostilbene. It is used as an intermediate or a starting material in the synthesis of many anticonvulsant drugs.
Packaging: 1, 5 g in glass bottle
Purity 97%
mp 196-199 °C (lit.)
UNSPSC 12352100

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