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Chemical Structure| 4442-85-7 Chemical Structure| 4442-85-7

Structure of 2-Cyclohexylethylamine
CAS No.: 4442-85-7

Chemical Structure| 4442-85-7

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Product Details of [ 4442-85-7 ]

CAS No. :4442-85-7
Formula : C8H17N
M.W : 127.23
SMILES Code : NCCC1CCCCC1
MDL No. :MFCD01734731
InChI Key :HFACYWDPMNWMIW-UHFFFAOYSA-N
Pubchem ID :20509

Safety of [ 4442-85-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 4442-85-7 ]

* 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 [ 4442-85-7 ]

[ 4442-85-7 ] Synthesis Path-Downstream   1~5

  • 2
  • [ 6975-71-9 ]
  • [ 4435-18-1 ]
  • [ 4435-14-7 ]
  • [ 4442-85-7 ]
  • [ 3399-73-3 ]
  • 3
  • [ 440627-14-5 ]
  • [ 4442-85-7 ]
  • C22H24N2O2S [ No CAS ]
YieldReaction ConditionsOperation in experiment
50% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 - 20℃; for 16h;Inert atmosphere; [000447] Synthesis of N-(2-cyclohexylethyl)- 1 1-oxo- 10, 1 1-dihydrodibenzo [b, J] [1, 4jthiazepine-8-carboxamide (545): To a stirred solution of 6 (100 mg, 0.36 mmol) in DMF (6mL) under argon atmosphere were added EDCI.HC1 (105 mg, 0.54 mmol), HOBt (74 mg, 0.54mmol), 2-cyclohexylethan-1-amine 261 (56 mg, 0.44 mmol), and diisopropyl ethyl amine (95 mg, 0.73 mmol) at 0-5 C; warmed to RT and stirred for 16 h. The reaction was monitored by TLC; after completion of the reaction, the volatiles were removed in vacuo. The residue was diluted with water (20 mL), filtered and washed with water (2 x 5 mL) to obtain the crude. The crude was triturated with EtOAc (2 x 5 mL) to afford 545 (70 mg, 50%) as white solid. TLC:5% MeOH/ CH2C12 (R 0.5); 1H-NMR (DMSO-d6, 400 MHz): oe 10.75 (s, 1H), 8.43 (t, J 5.6 Hz, 1H), 7.69-7.62 (m, 3H), 7.56-7.43 (m, 4H), 3.26-3.21 (m, 2H), 1.70-1.58 (m, 5H), 1.40-1.35 (m, 2H), 1.28-1.09 (m, 4H), 0.91-0.83 (m, 2H).
  • 4
  • [ 97-08-5 ]
  • [ 4442-85-7 ]
  • 4-chloro-N-(2-cyclohexylethyl)-3-nitrobenzenesulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% With pyridine; In dichloromethane; at 0 - 20℃; for 2h;Inert atmosphere; [000422] Synthesis of 4-chloro-N-(2-cyclohexylethyl)-3-nitrobenzenesulfonamide (529): Toa stirred solution of 2-cyclohexylethan-1-amine 261 (500 mg, 3.93 mmol) in CH2C12 (10 mL) under inert atmosphere were added pyridine (0.9 mL), 4-chloro-3-nitrobenzenesulfonyl chloride 528 (1 g, 3.93 mmol) at 0 C; warmed to RT and stirred for 2 h. The reaction was monitored by TLC; after completion of the reaction, the reaction mixture was diluted with water (20 mL) and extracted with CH2C12 (2 x 30 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo to obtain the crude. The crude was purified through silica gel column chromatography using 15% EtOAc/ hexanes to afford compound 529 (1.36 g, 52%) as yellow solid. TLC: 30% EtOAc/ hexanes (R 0.6); 1H-NMR (CDC13, 400 MHz): oe8.33 (s, 1H), 7.97 (d, J 8.4 Hz, 1H), 7.71 (d, J 8.4 Hz, 1H), 4.52 (t, J= 5.6 Hz, 1H), 3.03 (q, 2H), 1.69-1.56 (m, 4H), 1.40-1.35 (m, 2H), 1.28-1.08 (m, 5H), 0.89-0.83 (m, 2H).
  • 5
  • [ 23687-26-5 ]
  • [ 4442-85-7 ]
  • [ 530-62-1 ]
  • 1-(2-cyclohexylethyl)-3-(isoquinolin-6-yl)urea [ No CAS ]
 

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