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 CALL FOR PRICEAdd To Favorites		Add To Favorites
45-143650-5G	5 g	$129.00 1/EAAdd To Favorites		Add To Favorites

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

Symbol	GHS07,GHS09
Signal word	Warning
Hazard statements	H302 - H411
Precautionary statements	P273 - P301 + P312 + P330
Hazard Codes	Xn,N
Risk Statements	22-51/53
Safety Statements	61
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 2
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable