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[ CAS No. 3185-73-7 ] {[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
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 3185-73-7
Chemical Structure| 3185-73-7
Structure of 3185-73-7 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 3185-73-7 ]

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Alternatived Products of [ 3185-73-7 ]

Product Details of [ 3185-73-7 ]

CAS No. :3185-73-7 MDL No. :MFCD24141223
Formula : C13H9ClO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 232.66 Pubchem ID :-
Synonyms :

Safety of [ 3185-73-7 ]

Signal Word:Danger Class:6.1,8
Precautionary Statements:P501-P260-P270-P262-P234-P271-P264-P280-P284-P390-P361+P364-P303+P361+P353-P301+P330+P331-P301+P310+P330-P304+P340+P310-P305+P351+P338+P310-P403+P233-P406-P405 UN#:3277
Hazard Statements:H300+H310+H330-H314-H290 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 3185-73-7 ]

* 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 [ 3185-73-7 ]

[ 3185-73-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3185-73-7 ]
  • [ 71-43-2 ]
  • [ 2170-13-0 ]
  • 2
  • [ 3185-73-7 ]
  • [ 82241-22-3 ]
  • [ 1420814-46-5 ]
YieldReaction ConditionsOperation in experiment
0.2973 g With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; at 20℃; To a solution of triphosgene (0.099 g, 0.33 mmol, 0.33 eq) in CH2Cl2 (10 mL), was slowly added 4-hydroxybiphenyl (0.1702 g, 1 mmol, 1 eq) and N,N-diisopropylethylamine (DIEA) (176 muL, 0.130 g, 1 mmol, 1 eq) as a solution in THF (10 mL). The reaction was stirred at room temperature for 30 min to generate the intermediate chloroformate. In a separate flask containing CH2Cl2 (10 mL), 2-methyl-4- piperazinoquinoline (0.3410 g, 1.5 mmol, 1.5 eq) was mixed with DIEA (263 muL, 0.195 g, 1.5 mmol, 1.5 eq). The mixture was stirred for 5 min at room temperature and then dropped into the flask containing the chloroformate. The reaction mixture was stirred at room temperature for another 30 min and partitioned between CH2Cl2 (50 mL) and saturated NH4Cl (50 mL). The organic layer was washed one more time with saturated NH4Cl (30 mL), dried over MgSO4 and filtered. The solvent was removed by rotary evaporation and the product was purified by silica gel column chromatography (1:1 ethyl acetate/hexanes) to afford JMN4 (0.2973 g, 0.702 mmol, 70%).
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