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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 6728-26-3 Chemical Structure| 6728-26-3
Chemical Structure| 6728-26-3

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Trans-2-hexenal is an α,β-unsaturated carbonyl compound protecting plants against harmful substances.

Synonyms: Trans-2-Hexenal; Leaf aldehyde

4.5 *For Research Use Only !

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Product Details of trans-2-Hexenal

CAS No. :6728-26-3
Formula : C6H10O
M.W : 98.14
SMILES Code : CCC/C=C/C=O
Synonyms :
Trans-2-Hexenal; Leaf aldehyde
MDL No. :MFCD00007008
InChI Key :MBDOYVRWFFCFHM-SNAWJCMRSA-N
Pubchem ID :5281168

Safety of trans-2-Hexenal

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H302-H311-H317
Precautionary Statements:P280-P312
Class:3(6.1)
UN#:1988
Packing Group:

Application In Synthesis of trans-2-Hexenal

* 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 [ 6728-26-3 ]

[ 6728-26-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6728-26-3 ]
  • [ 309947-86-2 ]
  • C21H31N5O5 [ No CAS ]
  • 2
  • [ 6728-26-3 ]
  • [ 64-17-5 ]
  • [ 27829-72-7 ]
YieldReaction ConditionsOperation in experiment
With oxygen; at 100℃; under 3750.38 Torr; for 7h;Autoclave; General procedure: Octanal (128 mg, 1.00 mmol), ethanol (2 mL, 34.3 mmol), 1 wt% gold catalyst (100 mg, Au 0.5 mol%), tridecane as an internal standard, and a magnetic stirring bar was charged in an autoclave. Oxygen gas was filled in the autoclave with 0.5 MPa (the gauge pressure). The reaction was carried out at 100 C. After 5 h, the reaction mixture was extracted with ethanol and filtered. The filtrate was analyzed by gas chromatography using an Agilent7890A or a Shimadzu GC2014 with an HP-5 column.
 

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