Iminostilbene

Modify Date: 2024-01-05 14:16:29

Iminostilbene Structure
Iminostilbene structure
 Common Name Iminostilbene
CAS Number 256-96-2 Molecular Weight 193.244
Density 1.1±0.1 g/cm3 Boiling Point 349.1±22.0 °C at 760 mmHg
Molecular Formula C14H11N Melting Point 197 °C
MSDS Chinese USA Flash Point 178.4±17.8 °C
Symbol GHS07 GHS09
GHS07, GHS09		 Signal Word Warning

 Use of Iminostilbene


Iminostilbene is a a chemical precursor of carbamazepine[1].

 Names

Name 5H-dibenzo[b,f]azepine
Synonym More Synonyms

 Iminostilbene Biological Activity

Description Iminostilbene is a a chemical precursor of carbamazepine[1].
Related Catalog
References

[1]. Christian P, et al. Crystallization of Carbamazepine in Proximity to Its Precursor Iminostilbene and a Silica Surface. Cryst Growth Des. 2016 May 4;16(5):2771-2778. Epub 2016 Mar 30.

 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

 Safety Information

Symbol GHS07 GHS09
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

 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%

 Articles11

More Articles
Free-radical-scavenging effect of carbazole derivatives on AAPH-induced hemolysis of human erythrocytes.

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 ...
Simulation of the hepatic metabolism of stilbene and its tricyclic derivatives by Fenton and Ruff reagents: models for cytochrome P-450 activation of chemical carcinogens.

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...
Synthesis and antioxidant properties of some novel 5H-dibenz[b,f]azepine derivatives in different in vitro model systems.

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...

 Synonyms

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
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Related Compounds: More...
IMINOSTILBENE
51421-13-7
Iminostilbene-d2
1189918-57-7
o,o'-Iminostilbene
13341-72-5
N-Acetyl Iminostilbene
19209-60-0
10-Methoxyiminostilbene
4698-11-7
3-Methoxy Iminostilbene
92483-74-4
N-(chloropropyl)iminostilbene
51551-40-7
Iminostilbene Carbonyl Chloride
33948-22-0
IMinostilbene-10,11-dihydrodiol
56211-73-5
Chemsrc provides Iminostilbene(CAS#:256-96-2) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of Iminostilbene are included as well.>> amp version: Iminostilbene

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