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5H-???[b,f]???

5H-???[b,f]???
5H-???[b,f]??? ??? ???
?? ??:
256-96-2
???:
5H-???[b,f]???
???(??):
5H-???[b,f]???
???:
Iminostilbene
???(??):
5H-Dibenz[b,f]azepine;CarbaMazepine Related CoMpound B;Iminostilben;5H-Dibenz[b,f]azepin;5H-Dibenzo(b,f)azepine;R-FMOC;RP 9989;IminostiL;NSC 123458;Iminostilbene
CBNumber:
CB8853392
???:
C14H11N
??? ??:
193.24
MOL ??:
256-96-2.mol
MSDS ??:
SDS

5H-???[b,f]??? ??

???
197 °C
?? ?
221 °C(lit.)
??
1.290 g/mL at 20 °C(lit.)
???
n20/D 1.523(lit.)
???
>230 °F
?? ??
Keep in dark place,Sealed in dry,Room Temperature
???
???: 50mg/mL, ??
??? ??
??
?? ?? (pKa)
1.71±0.20(Predicted)
??
????? ?????
???
?? ?????(25 mg/ml), ?(??), ???, ????? ? DMSO? ?????.
BRN
1343358
InChI
1S/C14H11N/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)15-13/h1-10,15H
InChIKey
LCGTWRLJTMHIQZ-UHFFFAOYSA-N
SMILES
N1c2ccccc2C=Cc3ccccc13
LogP
4.06
CAS ??????
256-96-2(CAS DataBase Reference)
NIST
EPA
5H-Dibenz[b,f]azepine (256-96-2)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? C,Xi,N,Xn
?? ???? ?? 34-51/53-22-36/37/38
????? 26-36/37/39-45-61-27-24/25
????(UN No.) UN 3265 8/PG 2
WGK ?? 3
F ?????? 10-21
?? ?? ?? Irritant
HS ?? 29339900
???? ??? 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Aquatic Chronic 2
????(GHS): Exclamation Mark (GHS07)Environment (GHS09)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H302 ??? ??? ?? ?? ?? - ?? ?? 4 ?? P264, P270, P301+P312, P330, P501
H411 ??? ??? ?? ????? ??? ?? ????? ?? - ?? ?? 2
??????:
P273 ???? ???? ???.
NFPA 704
1
0 0

5H-???[b,f]??? MSDS


5H-Dibenz[b,f]azepine

5H-???[b,f]??? C??? ??, ??, ??

??? ??

Yellow to orange-yellow fine powder

??

Iminostilbene is mainly used as a pharmaceutical intermediate for the production of carbamazepine, Oxcarbazepine, and rhodium catalyst ligand. It is a metabolite of of carbamazepine which is used primarily in the treatment of epilepsy and neuropathic pain.

?? ??

iminostilbene synthesis: 10,11-Dihydro-5-dibenz(b,f)azepine [Iminodibenzyl, 494-19-9] as raw material was acylated by triphosgene, after bromination by bromine and dehydrobromination, reacted with sodium hydroxide in isopropanol to give Iminostilbene.

??

ChEBI: Iminostilbene is a mancude organic heterotricyclic parent that consists of a seven-membered nitrogen hetrocycle fused with two benzene rings. It has a role as a marine xenobiotic metabolite. It is a mancude organic heterotricyclic parent and a dibenzoazepine.

?? ??

Iminostilbene has good antioxidant effects. N-acetyl iminostilbene was synthesized by incubating iminostilbene (2.0020 g, 10.360 mmol) with acetic anhydride.

?? ??

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.It is also used as a starting material to prepare pharmacologically important dibenzoazepine-pyridazine derivatives and synthesize olefinic multidentate ligand, which is used to prepare Rh(I) complexes.

5H-???[b,f]??? ?? ?? ? ???

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?? ??


5H-???[b,f]??? ?? ??

???( 354)?? ??
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