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[ CAS No. 110703-94-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
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Chemical Structure| 110703-94-1
Chemical Structure| 110703-94-1
Structure of 110703-94-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 110703-94-1 ]

CAS No. :110703-94-1 MDL No. :MFCD00865476
Formula : C19H12F3N3O3S Boiling Point : -
Linear Structure Formula :- InChI Key :BCSVCWVQNOXFGL-UHFFFAOYSA-N
M.W : 419.38 Pubchem ID :1613
Synonyms :
CP73850

Safety of [ 110703-94-1 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P264-P270-P273-P301+P310+P330-P405-P501 UN#:2811
Hazard Statements:H301-H413 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 110703-94-1 ]

* 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 [ 110703-94-1 ]

[ 110703-94-1 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 110703-94-1 ]
  • 2-[4-Oxo-3-(5-trifluoromethyl-benzothiazol-2-ylmethyl)-3,4-dihydro-phthalazin-1-yl]-acetamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With ammonia; acetic anhydride 1.) reflux, overnight, 2.) Et2O, 10 deg C; Yield given. Multistep reaction;
  • 2
  • [ 110703-94-1 ]
  • [ 131105-76-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 1.) acetic anhydride, 2.) NH3(g) / 1.) reflux, overnight, 2.) Et2O, 10 deg C 2: 83 percent / POCl3 / CH2Cl2 / 6 h / Heating
  • 3
  • [ 110703-94-1 ]
  • [ 131105-77-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 1.) acetic anhydride, 2.) NH3(g) / 1.) reflux, overnight, 2.) Et2O, 10 deg C 2: 83 percent / POCl3 / CH2Cl2 / 6 h / Heating 3: 20 percent / NaN3, NH4Cl / dimethylformamide / 48 h / 120 °C
  • 4
  • [ 110703-94-1 ]
  • sodium 3,4-dihydro-4-oxo-3-((5-(trifluoromethyl)-2-benzothiazolyl)methyl)-1-phthalazineacetate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium methylate In methanol 18 Sodium 3-(5-trifluoromethylbenzothiazol-2-ylmethyl)-4-oxo-3H-phthalazin-1-ylacetate EXAMPLE 18 Sodium 3-(5-trifluoromethylbenzothiazol-2-ylmethyl)-4-oxo-3H-phthalazin-1-ylacetate Sodium methoxide (54 mg) was added to 3-(5-trifluoromethylbenzothiazol-2-ylmethyl)-4-oxo-phthalazin-1-ylacetic acid (0.4 g) in methanol 10 ml) at room temperature. After the addition was complete, a clear solution was obtained which was stirred for 15 minutes at room temperature. The excess methanol was evaporated. The residue was triturated with ether (20 ml) and filtered to obtain the product (0.43 g; m.p. 300° C.).
YieldReaction ConditionsOperation in experiment
A preferred subgroup within the above group of compounds includes numbered compounds 1, 2, 3, 4, 5, 6, 9, 10, and 17, and the following compounds of Formula I: ... 25. 3,4-dihydro-3-(5-fluorobenzoxazol-2-ylmethyl)-4-oxophthalazin-1-yl-acetic acid [R1=hydroxy; X=F; Y=H]; 26. 3-(5,7-difluorobenzoxazol-2-ylmethyl)-3,4-dihydro-4-oxophthalazin-1-ylacetic acid [R1=hydroxy; X=Y=F]; 27. 3-(5-chlorobenzoxazol-2-ylmethyl)-3,4-dihydro-4-oxophthalazin-1-ylacetic acid [R1=hydroxy; X=Cl; Y=H]; 28. 3-(5,7-dichlorobenzoxazol-2-ylmethyl)-3,4-dihydro-4-oxophthalazin-1-ylacetic acid [R1=hydroxy; X=Y=Cl]; and 29. zopolrestat; 1-phthalazineacetic acid, 3,4-dihydro-4-oxo-3-[[5-(trifluoromethyl)-2-benzothiazolyl]methyl]- [R1=hydroxy; X=trifluoromethyl; Y=H].
Preferred are pharmaceutical preparations containing at least one substituted 2-phenylbenzimidazole of formula IA or IA1 as well as an active substance selected from among: ... tolrestat, troglitazone, voglibose, zenarestat and zopolrestat.
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