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[ CAS No. 910875-39-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 910875-39-7
Chemical Structure| 910875-39-7
Structure of 910875-39-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 910875-39-7 ]

CAS No. :910875-39-7 MDL No. :MFCD18910964
Formula : C11H14ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 211.69 Pubchem ID :-
Synonyms :

Safety of [ 910875-39-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 910875-39-7 ]

* 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.

  • Upstream synthesis route of [ 910875-39-7 ]
  • Downstream synthetic route of [ 910875-39-7 ]

[ 910875-39-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 910875-39-7 ]
  • [ 24424-99-5 ]
  • [ 632352-56-8 ]
YieldReaction ConditionsOperation in experiment
5.46 g With triethylamine In acetonitrile for 14 h; The obtained powder of crude 7 (5.00 g, 23.6 mmol) was dissolved in a mixture of CH3CN (100 mL) and Et3N (4.94 mL, 35.4 mmol) and then di-tert-butoxycarbonate (7.73 g, 35.4 mmol) was slowly added thereto. After stirring for 14 h, the reaction mixture was concentrated in vacuo, and then the residue was dissolved in EtOAc and H2O. The organic layer was washed with aqueous NH4Cl and brine, dried and concentrated to provide 8 (5.46 g, 84percent) as white solids. 1H NMR (CDCl3) δ: 1.50 (9H, s), 2.57 (2H, t, J = 6.1 Hz), 3.45-3.74 (3H, m), 4.10-4.40 (2H, m), 7.15-7.21 (2H, m), 7.28-7.41 (3H, m).
Reference: [1] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 21, p. 6430 - 6446
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