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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 5807-14-7 Chemical Structure| 5807-14-7
Chemical Structure| 5807-14-7

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Synonyms: 1,5,7-Triazabicyclo[4.4.0]dec-5-ene; TBD

4.5 *For Research Use Only !

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Product Details of Triazabicyclodecene

CAS No. :5807-14-7
Formula : C7H13N3
M.W : 139.20
SMILES Code : C12=NCCCN1CCCN2
Synonyms :
1,5,7-Triazabicyclo[4.4.0]dec-5-ene; TBD
MDL No. :MFCD00043003
InChI Key :FVKFHMNJTHKMRX-UHFFFAOYSA-N
Pubchem ID :79873

Safety of Triazabicyclodecene

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:1759
Packing Group:

Application In Synthesis of Triazabicyclodecene

* 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 [ 5807-14-7 ]

[ 5807-14-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 5807-14-7 ]
  • [ 1186-73-8 ]
  • octahydro-pyrimido[1,2-a]pyrimidin-1-ium tris(methoxycarbonyl)methanide [ No CAS ]
  • 2
  • [ 5807-14-7 ]
  • [ 112270-06-1 ]
  • [ 106-95-6 ]
  • [ 379230-44-1 ]
YieldReaction ConditionsOperation in experiment
In acetonitrile; Petroleum ether; Allyl bromide (5.5 ml) was added to a stirred mixture of <strong>[112270-06-1]ethyl 6-chloro-2-hydroxybenzoate</strong> (9.8 g), 1,5,7-triazabicyclo[4,4,0]dec-5-ene (10.4 g) and acetonitrile (250 ml) and the reaction mixture was stirred at ambient temperature for 20 hours. The mixture was evaporated and the residue was purified by column chromatography on silica using a 17:3 mixture of petroleum ether (b.p. 60-80C) and diethyl ether as eluent. There was thus obtained ethyl 2-allyloxy-6-chlorobenzoate (10.3 g); NMR Spectrum : (DMSOd6) 1.3 (t, 3H), 4.35 (q, 2H), 4.65 (d, 2H), 5.25 (d, 1H), 5.4 (d, 1H), 6.0 (m, 1H), 7.15 (m, 2H), 7.45 (t, 1H).
In acetonitrile; Petroleum ether; Allyl bromide (5.5 ml) was added to a stirred mixture of <strong>[112270-06-1]ethyl 6-chloro-2-hydroxybenzoate</strong> (9.8 g), 1,5,7-triazabicyclo[4,4,0]dec-5-ene (10.4 g) and acetonitrile (250 ml) and the reaction mixture was stirred at ambient temperature for 20 hours. The mixture was evaporated and the residue was purified by column chromatography on silica using a 17:3 mixture of petroleum ether (b.p. 60-80 C.) and diethyl ether as eluent. There was thus obtained ethyl 2-allyloxy-6-chlorobenzoate (10.3 g); NMR Spectrum: (DMSOd6) 1.3 (t, 3H), 4.35 (q, 2H), 4.65 (d, 2H), 5.25 (d, 1H), 5.4 (d, 1H), 6.0 (m, 1H), 7.15 (m, 2H), 7.45 (t, 1H).
  • 3
  • [ 7089-68-1 ]
  • [ 5807-14-7 ]
  • mer-[Ru(2-hpp-1,10-phenanthroline)2][(PF6)2]·(ethyl acetate) [ No CAS ]
  • 4
  • [ 7089-68-1 ]
  • [ 5807-14-7 ]
  • 2-(hexahydro-pyrimidopyrimidine)-1,10-phenanthroline [ No CAS ]
 

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