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Chemical Structure| 40754-13-0 Chemical Structure| 40754-13-0

Structure of 40754-13-0

Chemical Structure| 40754-13-0

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Product Details of [ 40754-13-0 ]

CAS No. :40754-13-0
Formula : C14H15N3
M.W : 225.29
SMILES Code : NC1=CC=CC=C1/C(C)=N/NC2=CC=CC=C2
MDL No. :MFCD00799468

Safety of [ 40754-13-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 40754-13-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 40754-13-0 ]

[ 40754-13-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 40754-13-0 ]
  • [ 32566-01-1 ]
YieldReaction ConditionsOperation in experiment
58% With methanesulfonic acid; phosphorus pentoxide; at 80℃; for 0.5h; Methanesulfonic acid (70 mL) was stirred and heated to 80 oC. Phosphorus pentoxide (9.45 g,66.6 mmol) was added in one portion and the resulting suspension was stirred until ahomogeneous solution was formed (c.a. 5 min). After this time, 43 (7.00 g, 31.1 mmol) wasadded portionwise over 15 minutes. The reaction mixture was stirred at 80 oC for a further 30minutes and then cooled to room temperature an poured over a mixture of crushed ice (c.a.500 g) and sodium hydroxide pellets (45.5 g). A precipitate was formed, which was isolatedby vacuum filtration and washed with water (2 x 20 mL). The residue was purified viarecrystallization from ethanol to afford the title compound 13 as a beige solid (3.75 g, 58 %).The data matched that previously reported in the literature.8Melting point 146-148 oC (ethanol) [lit. 146 oC]; 81H NMR (400 MHz, d6-DMSO) = 11.27 (s, 1H, NH indole), 7.56 (d, J = 7.8 Hz, 1H, HAr),7.45-7.38 (m, 2H, HAr), 7.14-7.07 (m, 2H, HAr), 7.03 (t, J = 7.5 Hz, 1H, HAr), 6.87 (d, J = 8.1Hz, 1H, HAr), 6.75 (m, 2H, H7 and HAr), 5.22 (s, 2H, NH aniline);13C NMR (126 MHz, d6-DMSO) C = 146.1, 136.8, 136.6, 129.3, 129.1, 128.8, 121.5, 120.2,119.5, 117.6, 117.1, 116.2, 111.6, 100.4;FTIR (neat) /cm-1 = 3378, 3304, 3181, 1614, 1490, 1449, 1410, 1347, 1296, 1242, 1154;LRMS (ESI+) 209 ([M + H]+).
With hydrogenchloride;Zinc chloride; In ammonium hydroxide; b. Preparation of 2-(2'-amino-phenyl)-indole. An intimate mixture of 10 g (0.045 mol) of 2-amino-acetophenone-phenylhydrazone and 50 g of zinc chloride was heated to about 165 C. After a few minutes a homogeneous brownish liquid was obtained and was mixed and heated for 10 minutes. After standing for 30 minutes at room-temperature, the mixture was taken up with 10% hydrochloric acid and stirred until complete dissolution of the zinc chloride. The yellow suspension obtained was filtered and the crystals were washed with a minimum of cold water and then poured into 100 ml of 10% hydrochloric acid. The reaction medium was heated until a homogenous solution was obtained, after which the solution was filtered. The filtrate was cooled and taken up in ammonia hydrate until precipitation of a whitish substance. The reaction medium was centrifuged and the precipitate was washed several times with cold water. Purification was carried out twice and after two recrystallizations from toluene, 7.5 g of 2-(2'-amino-phenyl)-indole were obtained. M.P.: 156 C Yield: 76%
  • 2
  • [ 40754-13-0 ]
  • [ 399-25-7 ]
  • [ 1401404-45-2 ]
 

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