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[ CAS No. 1269667-51-7 ]

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Cat. No.: {[proInfo.prAm]}
2D
Chemical Structure| 1269667-51-7
Chemical Structure| 1269667-51-7
Structure of 1269667-51-7 *Storage: {[proInfo.prStorage]}

Quality Control of [ 1269667-51-7 ]

Related Doc. of [ 1269667-51-7 ]

SDS
Alternatived Products of [ 1269667-51-7 ]
Alternatived Products of [ 1269667-51-7 ]

Product Details of [ 1269667-51-7 ]

CAS No. :1269667-51-7MDL No. :MFCD19443913
Formula : C6H3BrClN3 Boiling Point : -
Linear Structure Formula :-InChI Key :N/A
M.W :232.47Pubchem ID :-
Synonyms :

Computed Properties of [ 1269667-51-7 ]

TPSA : - H-Bond Acceptor Count : -
XLogP3 : - H-Bond Donor Count : -
SP3 : - Rotatable Bond Count : -

Safety of [ 1269667-51-7 ]

Signal Word:WarningClass:N/A
Precautionary Statements:P261-P305+P351+P338UN#:N/A
Hazard Statements:H302-H315-H319-H335Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1269667-51-7 ]

  • Downstream synthetic route of [ 1269667-51-7 ]

[ 1269667-51-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 888720-29-4 ]
  • [ 1269667-51-7 ]
YieldReaction ConditionsOperation in experiment
83% With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 0℃; for 1.5h; To a solution of 4-chloropyrrolo[l,2-/J[l,2,4]triazine (3.00 g, 19.5 mmol; Leadgen Labs) in DMF (35 mL) was added N-bromosuccinimide (3.51 g, 19.7 mmol) at 0 C, and the reaction mixture was stirred at 0 C for 90 minutes. Subsequent dilution with ethyl acetate and addition of a saturated aqueous solution OfNaHCO3 is followed by separation of the layers. The organic layers were washed with water (3x), dried with sodium sulfate, filtered, and concentrated in vacuo. The crude product was purified by flash chromatography to afford7-bromo-4-chloropyrrolo[l,2-/][l,2,4]triazine (3.75 g, 83%).
  • 2
  • [ 122181-85-5 ]
  • [ 1269667-51-7 ]
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