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[ CAS No. 590417-56-4 ] {[proInfo.proName]}

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Chemical Structure| 590417-56-4
Chemical Structure| 590417-56-4
Structure of 590417-56-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 590417-56-4 ]

CAS No. :590417-56-4 MDL No. :MFCD12964857
Formula : C9H10BNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :GLLDFWAZHLTQLC-UHFFFAOYSA-N
M.W : 174.99 Pubchem ID :22558942
Synonyms :

Safety of [ 590417-56-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 590417-56-4 ]

* 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 [ 590417-56-4 ]

[ 590417-56-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 590417-55-3 ]
  • [ 590417-56-4 ]
YieldReaction ConditionsOperation in experiment
Stage #1: 4-bromo-1-methyl-1H-indole With n-butyllithium In tetrahydrofuran; pentane at -78℃; for 1h; Stage #2: With Triisopropyl borate In tetrahydrofuran; pentane at 20℃; for 4h; 121 Synthesis of 1-methyl-1H-indole-4-boronic Acid (Intermediate 52) Synthesis of 1-methyl-1H-indole-4-boronic Acid (Intermediate 52) A solution of Intermediate 51 (4.90 g) in anhydrous THF (30 ml) was cooled to -78° C. under argon atmosphere, then added dropwise with 1.62 M solution of n-butyllithium in pentane (28.8 ml) over 30 minutes and stirred for 30 minutes.The mixture was added dropwise with (iPrO)3B (10.77 ml) over 10 minutes, stirred for 1 hour, then warmed to room temperature and further stirred for 2.5 hours.The reaction mixture was poured into 1.2 N aqueous phosphoric acid (250 ml) added with ice, and extracted with diethyl ether (200 ml*3).The organic layer was extracted with 0.4 N aqueous sodium hydroxide (150 ml*3), and the aqueous layer was acidified with 5 N aqueous hydrochloric acid under ice cooling and extracted with diethyl ether (200 ml*3) again.The organic layer was washed with saturated brine and dried, and then the solvent was evaporated under reduced pressure.The residue was washed with hexane to obtain the title compound (Intermediate 52, 3.17 g).
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