143650

5H-Dibenz[b,f]azepine

97%

• 동의어(들): Iminostilbene
• 실험식(Hill 표기법): C₁₄H₁₁N
• CAS Number: 256-96-2
• Molecular Weight: 193.24
• Beilstein: 1343358
• EC Number: 205-970-0
• MDL number: MFCD00005071
• UNSPSC 코드: 12352100
• PubChem Substance ID: 24848600
• NACRES: NA.22

속성

• Quality Level: 200
• 분석: 97%
• mp: 196-199 °C (lit.)
• solubility: ethyl acetate: soluble 25 mg/mL, clear, yellow to orange
• SMILES string: N1c2ccccc2C=Cc3ccccc13
• 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

설명

일반 설명

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.

애플리케이션

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.

생화학적/생리학적 작용

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.

안전성 정보

• 픽토그램: GHS07,GHS09
• 신호어: Warning
• 유해 및 위험 성명서: H302,H411
• 예방조치 성명서: P273 - P301 + P312 + P330
• Hazard Classifications: Acute Tox. 4 Oral - Aquatic Chronic 2
• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 2
• Flash Point (°F): Not applicable
• Flash Point (°C): Not applicable
• 개인 보호 장비: dust mask type N95 (US), Eyeshields, Gloves