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Chemical Structure| 168409-55-0 Chemical Structure| 168409-55-0

Structure of 168409-55-0

Chemical Structure| 168409-55-0

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Product Details of [ 168409-55-0 ]

CAS No. :168409-55-0
Formula : C9H12N2
M.W : 148.21
SMILES Code : CC1=CC=CC2=C1NCCN2
MDL No. :MFCD24229011

Safety of [ 168409-55-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 168409-55-0 ]

* 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 [ 168409-55-0 ]

[ 168409-55-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 13708-12-8 ]
  • [ 168409-55-0 ]
YieldReaction ConditionsOperation in experiment
99%Chromat. With hydrogen; In methanol; water; at 80℃; under 7500.75 Torr; for 8h;Autoclave; Green chemistry; General procedure: In a typical run, a 50 mL stainless steel autoclave equipped with a transducer for online pressure monitoring was charged, under air, of Pd-pol (23.2 mg, Pd: 0.5 mol%), the substrate (1.0 mmol), and water (5.0 mL) or water (4.0 mL) and CH3OH (1.0 mL). The autoclave was then purged three times with hydrogen, then pressurized with 10 bar H2, set on a magnetic stirrer and heated to 80 C. After the minimum time needed to reach reaction completion, the autoclave was let to reach room temperature, the hydrogen was vented and the autoclave opened. The catalyst was recovered by filtration while the organic product was extracted with ethyl acetate (3 mL), the water phase was washed with ethyl acetate (2 × 5 mL) and the organic layers were collected. The yields were assessed by GLC analysis of the ethyl acetate solution with the internal standard (biphenyl) method.
86%Chromat. With sodium tetrahydroborate; water; at 60℃; for 9h;Inert atmosphere; General procedure: 2.2.2. Procedure A: 1.0 mmol of substrate, 37.2 mg of Pd-pol (Pd%w= 5.0,0.0175 mmol of Pd) and 20.0 mmol of sodium borohydride were stirred under nitrogen at 60C in 5 mL of double deionized water for the appropriate amount of time, using a three-necked flask equipped with a reflux condenser and a gas bubbler in order to discharge the hydrogen excess produced during reaction. The progress of the reaction was monitored by GLC. After completion of the reaction, the reaction mixture was centrifuged to separate the catalyst. The solid residue was first washed with deionized water and then with acetone and diethyl ether to remove any traces of organic material. The filtrate containing the reaction mixture was extracted with ethyl acetate (3 × 5 mL) and then dried over anhydrous Na2SO4. The solvent was evaporated under reduced pressure to yield the crude product, which was then purified by flash column chromatography using silica gel and an appropriate eluent (Supporting information) to afford the pure product. The products were characterized by GC-MS or 1H NMR by comparison with authentic samples. For the assessment of the chromatographic yields, biphenyl (50.0 mg) was used as the internal standard.
 

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