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[ CAS No. 131864-67-0 ] {[proInfo.proName]}

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Chemical Structure| 131864-67-0
Chemical Structure| 131864-67-0
Structure of 131864-67-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 131864-67-0 ]

CAS No. :131864-67-0 MDL No. :MFCD01321334
Formula : C17H23N3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :CSGQGLBCAHGJDR-GJZGRUSLSA-N
M.W : 301.38 Pubchem ID :688213
Synonyms :

Safety of [ 131864-67-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 131864-67-0 ]

* 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 [ 131864-67-0 ]

[ 131864-67-0 ] Synthesis Path-Downstream   1~20

  • 1
  • [ 131864-67-0 ]
  • rhodium(III) chloride trihydrate [ No CAS ]
  • {2,6-bis{4'-(R)-isopropyloxazolin-2'-yl}pyridine} rhodium trichloride [ No CAS ]
  • 2
  • [ 131864-67-0 ]
  • [ 3375-31-3 ]
  • [Pd(OCOCH3)((CH3)2CHC3H3NOC5H3NC(O)NCH(CH(CH3)2)CH2OCOCH3)] [ No CAS ]
  • ((R,R)-2,6-bis(4-isopropyl-2-oxazolin-2-yl)pyridine)Pd(OAc)2 [ No CAS ]
  • 3
  • [ 131864-67-0 ]
  • [ 152782-80-4 ]
  • LiCH2SiMe3 [ No CAS ]
  • [((R,R)-NC5H3(COCH2CH(i-Pr)N)2)Fe(CH2SiMe3)2] [ No CAS ]
  • 4
  • [ 131864-67-0 ]
  • tris(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)europium(III) [ No CAS ]
  • [Eu((R,R)-2,6-bis(4-isopropyl-2-oxazolin-2-yl)pyridine)(1,1,1,5,5,5-hexafluoropentane-2,4-dione-H)3] [ No CAS ]
  • 5
  • [ 131864-67-0 ]
  • tris(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)terbium(III) [ No CAS ]
  • [Tb((R,R)-2,6-bis(4-isopropyl-2-oxazolin-2-yl)pyridine)(1,1,1,5,5,5-hexafluoropentane-2,4-dione-H)3] [ No CAS ]
  • 6
  • [ 131864-67-0 ]
  • tris(3-trifluoroacetyl-d-camphorato)europium(III) [ No CAS ]
  • tris(3-trifluoroacetyl-d-camphorato)europium(III) 2,6-bis(4R-isopropyl-2-oxazolin-2-yl)pyridine [ No CAS ]
  • 7
  • [ 131864-67-0 ]
  • europium(III) nitrate hexahydrate [ No CAS ]
  • tetrabutylammonium octacyanidotungstate(V) [ No CAS ]
  • [ 68-12-2 ]
  • [EuIII((R,R)-2,2'-(2,6-pyridinediyl)bis(4-isopropyl-2-oxazoline))(dmf)4]3[WV(CN)8]3}n*dmf*8H2O [ No CAS ]
  • 8
  • [ 131864-67-0 ]
  • gadolinium(III) nitrate hexahydrate [ No CAS ]
  • [{(C4H9)4N}3W(CN)8] [ No CAS ]
  • [ 68-12-2 ]
  • [GdIII(R,R-2,6-bis(4-isopropyl-2-oxazolin-2-yl)pyridine)(dmf)4]3[WV(CN)8]3}n*dmf*4H2O [ No CAS ]
  • 9
  • [ 131864-67-0 ]
  • neodymium(III) nitrate hexahydrate [ No CAS ]
  • [{(C4H9)4N}3W(CN)8] [ No CAS ]
  • [ 68-12-2 ]
  • [NdIII(R,R-2,6-bis(4-isopropyl-2-oxazolin-2-yl)pyridine)(dmf)4]3[WV(CN)8]3}n*dmf*4H2O [ No CAS ]
  • 10
  • [ 131864-67-0 ]
  • tris-(dibenzoylmethanido) europium(III) [ No CAS ]
  • [Eu(1,3-diphenyl-1,3-propanedionato)3(R)-(2,6-bis(isopropyl-2-oxazolin-2-yl)pyridine)] [ No CAS ]
  • 11
  • iron(II) perchlorate hexahydrate [ No CAS ]
  • [ 131864-67-0 ]
  • [ 118949-61-4 ]
  • C34H46FeN6O4(2+)*2ClO4(1-) [ No CAS ]
  • 12
  • iron(II) perchlorate hexahydrate [ No CAS ]
  • [ 131864-67-0 ]
  • C34H46FeN6O4(2+)*2ClO4(1-) [ No CAS ]
  • 13
  • [ 131864-67-0 ]
  • zinc(II) bis(tetrafluoroborate) hydrate [ No CAS ]
  • C34H44N6O4Zn(2+)*2BF4(1-) [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% In acetonitrile; at 20℃; for 1h; (R)-LiPr (50mg, 0.17mmol) was dissolved in acetonitrile (15cm3). Zinc(II) tetrafluoroborate hydrate (20mg, 0.083mmol) was then added and the solution stirred at room temperature for one hour. A large excess of diethyl ether was added and the resultant precipitate was isolated by vacuum filtration leaving a white powder. Single crystals suitable for X-ray diffraction analysis were grown by vapour diffusion of diethyl ether into a concentrated solution of the product in acetonitrile. Yield: 0.054g, 78%. Elemental microanalysis: found C, 48.4; H, 5.39; N, 10.0%: calcd for C34H46B2F8N6O4Zn C, 48.5; H, 5.51; N, 9.98%. 1H NMR (CD3CN): delta 0.52 (d, 12H, 6.7Hz, iPr CH3), 0.64 (d, 12H, 6.7Hz, iPr CH3), 1.40 (dq, 4H, 13.4, 6.7Hz, iPr CH), 3.89 (ddd, 4H, 10.0, 8.7, 6.6Hz, ox-H), 4.67 (t, 4H, 8.9Hz, ox-H), 4.97 (t, 4H, 9.7Hz, ox-H), 8.41 (d, 4H, 7.9Hz, Py H3/5), 8.66 (t, 2H, 7.9Hz, Py H4).
  • 14
  • [ 131864-67-0 ]
  • zinc(II) bis(tetrafluoroborate) hydrate [ No CAS ]
  • [ 118949-61-4 ]
  • C34H46N6O4Zn(2+)*2BF4(1-) [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% In acetonitrile; at 20℃; for 1h; General procedure: (R)-LiPr (50mg, 0.17mmol) was dissolved in acetonitrile (15cm3). Zinc(II) tetrafluoroborate hydrate (20mg, 0.083mmol) was then added and the solution stirred at room temperature for one hour. A large excess of diethyl ether was added and the resultant precipitate was isolated by vacuum filtration leaving a white powder. Single crystals suitable for X-ray diffraction analysis were grown by vapour diffusion of diethyl ether into a concentrated solution of the product in acetonitrile. Yield: 0.054g, 78%.
  • 15
  • [ 131864-67-0 ]
  • cobalt(II) tetrafluoroborate hydrate [ No CAS ]
  • C34H44CoN6O4(2+)*2BF4(1-) [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% In acetonitrile; at 20℃; for 1h; General procedure: (R)-LiPr (50mg, 0.17mmol) was dissolved in acetonitrile (15cm3). Zinc(II) tetrafluoroborate hydrate (20mg, 0.083mmol) was then added and the solution stirred at room temperature for one hour. A large excess of diethyl ether was added and the resultant precipitate was isolated by vacuum filtration leaving a white powder. Single crystals suitable for X-ray diffraction analysis were grown by vapour diffusion of diethyl ether into a concentrated solution of the product in acetonitrile. Yield: 0.054g, 78%.
  • 16
  • [ 131864-67-0 ]
  • cobalt(II) tetrafluoroborate hydrate [ No CAS ]
  • [ 118949-61-4 ]
  • C34H46CoN6O4(2+)*2BF4(1-) [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% In acetonitrile; at 20℃; for 1h; General procedure: (R)-LiPr (50mg, 0.17mmol) was dissolved in acetonitrile (15cm3). Zinc(II) tetrafluoroborate hydrate (20mg, 0.083mmol) was then added and the solution stirred at room temperature for one hour. A large excess of diethyl ether was added and the resultant precipitate was isolated by vacuum filtration leaving a white powder. Single crystals suitable for X-ray diffraction analysis were grown by vapour diffusion of diethyl ether into a concentrated solution of the product in acetonitrile. Yield: 0.054g, 78%.
  • 17
  • tris(4,4,4-trifluoro-1-phenyl-1,3-butanedionato)europium [ No CAS ]
  • [ 131864-67-0 ]
  • ((R,R)-2,6-bis(4-isopropyl-2-oxazolin-2-yl)pyridine)(4,4,4-trifluoro-1-(4-phenyl)butane-1,3-dionate)3Eu [ No CAS ]
  • 18
  • [ 131864-67-0 ]
  • tris(furoyltrifluoroacetonato)europium(III) [ No CAS ]
  • ((R,R)-2,6-bis(4-isopropyl-2-oxazolin-2-yl)pyridine)(4,4,4-trifluoro-1-(2-furyl)butane-1,3-dionate)3Eu [ No CAS ]
  • 19
  • [ 131864-67-0 ]
  • Yb(2-thenoyltrifluoroacetonate)3·2H2O [ No CAS ]
  • Yb(2-thenoyltrifluoroacetonate)<SUB>3</SUB>(R,R)-<SUP>i</SUP>Pr(pyridine bisoxazoline) [ No CAS ]
  • 20
  • [ CAS Unavailable ]
  • [ 131864-67-0 ]
  • [ 123640-38-0 ]
  • [ 2765330-68-3 ]
YieldReaction ConditionsOperation in experiment
59% In acetonitrile at 20℃; for 2h;
Same Skeleton Products
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