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Chemical Structure| 73-34-7 Chemical Structure| 73-34-7

Structure of 73-34-7

Chemical Structure| 73-34-7

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Product Details of [ 73-34-7 ]

CAS No. :73-34-7
Formula : C6H12O5
M.W : 164.16
SMILES Code : OC1[C@@H]([C@@H]([C@H]([C@H](C)O1)O)O)O
MDL No. :N/A

Safety of [ 73-34-7 ]

Application In Synthesis of [ 73-34-7 ]

* 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.

  • Downstream synthetic route of [ 73-34-7 ]

[ 73-34-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 520-26-3 ]
  • [ 2280-44-6 ]
  • [ 73-34-7 ]
  • hesperetin 7‐O‐β‐D‐glucopyranoside [ No CAS ]
  • [ 520-33-2 ]
  • 2
  • [ 73-34-7 ]
  • [ 37091-73-9 ]
  • C11H21N2O5(1+)*Cl(1-) [ No CAS ]
  • 3
  • [ 520-26-3 ]
  • [ 73-34-7 ]
  • hesperetin 7‐O‐β‐D‐glucopyranoside [ No CAS ]
YieldReaction ConditionsOperation in experiment
With alpha-L-rhamnosidase from Fusarium moniliforme MTCC-2088; water; In aq. phosphate buffer; at 30℃;pH 10.5;Enzymatic reaction; General procedure: This experiment was performed in 1.0 mL solution of 1.0mM naringinin 0.5M sodium phosphate buffer pH 10.5 at 30 C. 25 muL purifiedenzyme stock (0.30 U/mL) was added. The reaction solution was leftovernight and the release of prunin was detected by thin layer chromatographyusing silica gel on glass plates and using butanol:aceticacid:water (40:11:29) (v/v) as mobile phase. The detection was madeusing the iodine chamber. Similar experiments were performed withrutin and <strong>[520-26-3]hesperidin</strong>. Preparative TLC in silica gel on glass plates wereused for purifying the enzymatic hydrolysis products of naringin, rutinand <strong>[520-26-3]hesperidin</strong> for HPLC-Mass spectrometric analysis. The HPLC-MassSpectrometric analysis was done at Sophisticated Analysis InstrumentCentre, CDRI, Lucknow, U.P. (India). The release of L-rhamnose wasalso detected by the thin layerchromatography using silica gel on glassplate and chloroform: methanol (70:30) (v/v) as the mobile phase. TheL-rhamnose released as the results of enzymatic hydrolysis of naringin,rutin and <strong>[520-26-3]hesperidin</strong> also was purified by preparative TLC and wasanalyzed by HPLC-Mass Spectrophotometric studies.
 

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