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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 2806-84-0 Chemical Structure| 2806-84-0

Structure of 2806-84-0

Chemical Structure| 2806-84-0

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Product Details of [ 2806-84-0 ]

CAS No. :2806-84-0
Formula : C4H8O2
M.W : 88.11
SMILES Code : O=CCCOC
MDL No. :MFCD08704314
InChI Key :OXGJKCALURPRCN-UHFFFAOYSA-N
Pubchem ID :137720

Safety of [ 2806-84-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H302-H315-H319-H335
Precautionary Statements:P210-P261-P305+P351+P338
Class:3
UN#:1993
Packing Group:

Application In Synthesis of [ 2806-84-0 ]

* 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 [ 2806-84-0 ]

[ 2806-84-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56-81-5 ]
  • [ 4740-78-7 ]
  • [ 2806-84-0 ]
  • [ 75-07-0 ]
  • [ 116-09-6 ]
  • [ 107-02-8 ]
YieldReaction ConditionsOperation in experiment
With H-ZSM5; In water; at 340℃; under 760.051 Torr; for 6.0h;Inert atmosphere; General procedure: For each experiment, 5 g of catalyst was charged into the reactorequipped with a catalyst support (stainless steel) and a fritted disk(quartz). Dimensions are reported in previously published work [5].Experiments were conducted at atmospheric pressure and 340 C in continuous operation with nitrogen as carrier gas and a con-stant supply of a 35 wt% glycerol aqueous solution. Details on massflow controllers, furnaces and pumps are described elsewhere [26].Sampling took place at hourly intervals, and product analyses wereoff-line. Liquid samples were collected using a syringe. Methanol was used as solvent for GC-MS analyses, performed in an Agilent6890 series GC with an Agilent 5973N detector and a Restek Rtx-200 MS column: 30 m × 0.25 mm ID × 0.5 m. Helium was used ascarrier gas with a sample injection (1 l) split ratio of 10:1 appliedfor all analyses. Injector and detector were maintained at 220Cand 285C respectively, while the oven initial temperature (45C)was held for 5 min, increasing to 115C in 15 min and then ramping up to 285C at a rate of 10C min-1. Filament and detector were turned off during the elution of the injection solvent (i.e. methanol).For quantification, cyclohexanone was used as internal standardand GC-FID analyses were conducted in a 5890A model GC, fitted with a Restek Stabilwax column: 30 m × 0.32 mm ID × 1 m, usingair, hydrogen and helium with a split ratio of 100:1. Injector anddetector were kept at 300C and 320C respectively, while an ini-tial temperature of 35C was held for 5 min, ramping to 200C ata rate of 10C min-1, holding at this temperature for 20 min. Gassamples were collected in a gas bag and analysed using a Varian490-GC micro gas chromatograph and an IR Prestige 21 ShimadzuFTIR QP 5000 apparatus. IR spectra were processed using QASoft software.
 

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