5-Amino-2-phenylindole
- Product Name
- 5-Amino-2-phenylindole
- CAS No.
- 6855-64-7
- Chemical Name
- 5-Amino-2-phenylindole
- Synonyms
- 5-Amino-2-phenylindole;2-phenyl-1H-indol-5-aMine;1H-Indol-5-amine, 2-phenyl-
- CBNumber
- CB02507594
- Molecular Formula
- C14H12N2
- Formula Weight
- 208.26
- MOL File
- 6855-64-7.mol
5-Amino-2-phenylindole Property
- Melting point:
- 231.5-233 °C(Solv: benzene (71-43-2))
- Boiling point:
- 469.3±25.0 °C(Predicted)
- Density
- 1.229±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 17.19±0.30(Predicted)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P310Immediately call a POISON CENTER or doctor/physician.
N-Bromosuccinimide Price
- Product number
- CHM0388559
- Product name
- 2-PHENYL-1H-INDOL-5-AMINE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $495.04
- Updated
- 2021/12/16
- Product number
- 0590AC
- Product name
- 2-Phenyl-1H-indol-5-amine
- Packaging
- 5g
- Price
- $1152
- Updated
- 2021/12/16
- Product number
- CM132610
- Product name
- 2-phenyl-1H-indol-5-amine
- Purity
- 95+%
- Packaging
- 10g
- Price
- $1388
- Updated
- 2021/12/16
- Product number
- CD11072517
- Product name
- 2-Phenyl-1H-indol-5-amine
- Purity
- 97%
- Packaging
- 10g
- Price
- $1471
- Updated
- 2021/12/16
- Product number
- H3766
- Product name
- 2-phenyl-1H-Indol-5-amine
- Purity
- 97.00%
- Packaging
- 1G
- Price
- $2460
- Updated
- 2021/12/16
5-Amino-2-phenylindole Chemical Properties,Usage,Production
Synthesis
4993-87-7
6855-64-7
Under nitrogen protection, 5-nitro-2-phenyl-1H-indole (2.83 g, 10 mmol) was dissolved in methanol (30 mL) and Raney Ni catalyst (510 mg) was added. The reaction mixture was placed under hydrogen atmosphere (1 atm) and the reaction was stirred at room temperature overnight. Upon completion of the reaction, the catalyst was removed by filtration through a diatomaceous earth pad and the filtrate was concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=5:1) to afford 2-phenyl-1H-indol-5-amine (1.6 g, 77% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3) and mass spectrometry (ESI): 1H NMR δ 7.76 (d, J=7.6 Hz, 2H), 7.39 (t, J=7.6 Hz, 2H), 7.24 (t, J=7.6 Hz, 1H), 7.07 (d, J=8.4 Hz, 1H), 6.64 (d, J=1.6 Hz, 1H), 6.60 (d, J=1.2 Hz, 1H), 6.48 (dd, J=2.0,8.4 Hz, 1H), 4.48 (brs, 2H); MS (ESI) m/e 209.0 ([M+H]+).
References
[1] Tetrahedron Letters, 2002, vol. 43, # 43, p. 7699 - 7702
[2] Journal of Medicinal Chemistry, 2010, vol. 53, # 10, p. 4085 - 4093
[3] Patent: US2007/244159, 2007, A1. Location in patent: Page/Page column 120
[4] Patent: US2011/98311, 2011, A1
[5] Patent: US2015/231142, 2015, A1. Location in patent: Paragraph 1672
5-Amino-2-phenylindole Preparation Products And Raw materials
Raw materials
Preparation Products
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