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Chemical Structure| 4748-78-1 Chemical Structure| 4748-78-1
Chemical Structure| 4748-78-1

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CAS No.: 4748-78-1

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4-Ethylbenzaldehyde is an endogenous metabolite, an aromatic aldehyde commonly used in organic synthesis and the fragrance industry.

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Product Details of 4-Ethylbenzaldehyde

CAS No. :4748-78-1
Formula : C9H10O
M.W : 134.18
SMILES Code : O=CC1=CC=C(CC)C=C1
MDL No. :MFCD00006956
InChI Key :QNGNSVIICDLXHT-UHFFFAOYSA-N
Pubchem ID :20861

Safety of 4-Ethylbenzaldehyde

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

Application In Synthesis of 4-Ethylbenzaldehyde

* 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 [ 4748-78-1 ]

[ 4748-78-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 288-16-4 ]
  • [ 4748-78-1 ]
  • [ 90672-85-8 ]
  • 2
  • [ 2899-28-7 ]
  • [ 4748-78-1 ]
  • [ 1227610-53-8 ]
  • [ 1237821-46-3 ]
  • 3
  • [ 1986-47-6 ]
  • [ 4748-78-1 ]
  • (1S*,2R*)-N-(4-ethylbenzyl)-2-phenylcyclopropan-1-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
34% General procedure: Trans-2-phenylcyclopropylamine hydrochloride (1.0 eq.), acetic acid (1.0eq.) and the appropriate aldehyde (0.9 eq.) were dissolved in around bottom flask in 10 mL dry DCE. The reaction mixture was stirred gently at room temperature for 2 h before sodium triacetoxyborohydride (3.0 eq.) was added in small portions to the reaction vessel. The reaction was monitored by TLC and quenched using 10 mL of an aqueous (5%) NaHCO3 solution. The organic layer was separated and the aqueous layer extracted three times with10 mL of DCE. All organic layers were combined, dried over anhydrous Na2SO4, concentrated in vacuo and purified using flash chromatography (silica gel; cyclohexane/ethyl acetate) to give the desired compound.
  • 4
  • [ 4748-78-1 ]
  • [ 68857-86-3 ]
 

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