Iminostilbene
Suppliers
Names
[ CAS No. ]:
256-96-2
[ Name ]:
Iminostilbene
[Synonym ]:
dibenz[b,f]azepine
MFCD00799229
Minostilbene
EINECS 249-478-4
5H-Dibenz[b,f]azepine
2,2'-Iminostilbense
Iminostilbene
Iminostilben
R-FMOC
5H-Dibenzo[b,f]azepine
dibenzazepine
5H-DIBENZ(B,F)AZEPINE
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
349.1±22.0 °C at 760 mmHg
[ Melting Point ]:
197 °C
[ Molecular Formula ]:
C14H11N
[ Molecular Weight ]:
193.244
[ Flash Point ]:
178.4±17.8 °C
[ Exact Mass ]:
193.089142
[ PSA ]:
12.03000
[ LogP ]:
4.11
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.627
[ Storage condition ]:
Refrigerator
[ Water Solubility ]:
dioxane: 50 mg/mL, clear
MSDS
Safety Information
[ Symbol ]:
GHS07, GHS09
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302-H411
[ Precautionary Statements ]:
P273
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xn:Harmful
[ Risk Phrases ]:
R22;R51/53
[ Safety Phrases ]:
S26-S36/37/39-S45-S61
[ RIDADR ]:
UN 3265 8/PG 2
[ WGK Germany ]:
3
[ HS Code ]:
2933990090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933990090
[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Bioorg. Med. Chem. 15 , 1903-13, (2007)
Since the research on antioxidants provides theoretical information for the medicinal development, and supplies some in vitro methods for quick-optimizing drugs, it attracts more scientific attention ...
Biopharm. Drug Dispos. 11(1) , 39-51, (1990)
Reactions of trans-stilbene, cis-stilbene, 5H-dibenzo [a,d] cyclo-heptene 5-one and 5H-dibenz [b,f] azepine (iminostilbene) with Fenton reagent [Fe (II)/H2O2] clearly simulate their hepatic metabolism...
Eur. J. Med. Chem. 45 , 2-10, (2010)
A series of 5H-dibenz[b,f]azepine containing different aminophenols and substituted aminophenols were synthesized. 3-chloro-1-(5H-dibenz[b,f]azepine-5yl)propan-1-one (2) was obtained by N-acylation of...