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[ CAS No. 35929-79-4 ] {[proInfo.proName]}

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Chemical Structure| 35929-79-4
Chemical Structure| 35929-79-4
Structure of 35929-79-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 35929-79-4 ]

CAS No. :35929-79-4 MDL No. :MFCD00087104
Formula : C19H22ClNO4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 363.84 Pubchem ID :-
Synonyms :

Safety of [ 35929-79-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P302+P352-P332+P313-P362-P301+P312+P330-P304+P340+P312-P403+P233-P405 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 35929-79-4 ]

* 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 [ 35929-79-4 ]
  • Downstream synthetic route of [ 35929-79-4 ]

[ 35929-79-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 35929-79-4 ]
  • [ 105-45-3 ]
  • [ 73257-49-5 ]
YieldReaction ConditionsOperation in experiment
91% With ammonium hydroxide In ethanol at 110℃; Flow reactor General procedure: Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate (4a). EtOH solution (3 mL) ofbenzaldehyde (0.67 M) mixed with ethyl acetoacetate (1.34 M) and the 25percent aqueous NH3 (3 mL) wererespectively transferred into gas-tight syringe 1 and syringe 2. The syringes were placed in a LongerLSP02-1B syringe pump which was set to deliver the reactants into the mixer at identical flow rate of 6.7μL/min. The reaction mixture was then allowed to flow through a stainless steel tube reactor which wasdipped in a 110 C oil bath. The output mixture was collected in a cooled sample vial. After reactioncompletion, rinsed the reactor with ethanol to collect all of the reactant solution and then concentratedunder vacuum. The residue was subjected to silica gel column chromatography with Pet-EA (5:1) aseluent to give 4a (612mg, 93percent yield).
Reference: [1] Heterocycles, 2016, vol. 93, # 2, p. 755 - 761
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