Home Cart 0 Sign in  

[ CAS No. 125708-66-9 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 125708-66-9
Chemical Structure| 125708-66-9
Structure of 125708-66-9 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 125708-66-9 ]

Related Doc. of [ 125708-66-9 ]

Alternatived Products of [ 125708-66-9 ]

Product Details of [ 125708-66-9 ]

CAS No. :125708-66-9 MDL No. :MFCD14705057
Formula : C7H9NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 139.15 Pubchem ID :-
Synonyms :

Safety of [ 125708-66-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P270-P273-P301+P312+P330-P501 UN#:N/A
Hazard Statements:H302-H412 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 125708-66-9 ]

* 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 [ 125708-66-9 ]

[ 125708-66-9 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 1609393-90-9 ]
  • [ 125708-66-9 ]
YieldReaction ConditionsOperation in experiment
57% With sodium perborate; water In tetrahydrofuran at 20℃; 5.1.2.8 3-Amino-2-methoxyphenol (46h) To a solution of 49h (358 mg, 1.44 mmol) in THF (10 mL) was added water (5 mL) and sodium perborate (569 mg, 3.7 mmol). The mixture was stirred at ambient temperature overnight. Excess THF was removed under reduced pressure. The residue was stirred with sat. NH4Cl solution (10 mL) and DCM (50 mL) for 1 h, then separated. The organics were concentrated under reduced pressure and purified by flash column chromatography, eluting with 0-60% EtOAc in isohexane, to return 46h (120 mg, 57%) as an off-white solid. 1H NMR (300 MHz, DMSO-d6) δ 8.80 (s, 1H), 6.55 (t, J = 7.84 Hz, 1H), 6.12 (d, J = 7.95 Hz, 1H), 6.05 (d, J = 7.77 Hz, 1H), 4.71 (s, 2H), 3.62 (s, 3H).
  • 3
  • sodium perborate [ No CAS ]
  • [ 1609393-90-9 ]
  • [ 7732-18-5 ]
  • [ 125708-66-9 ]
YieldReaction ConditionsOperation in experiment
125 mg In tetrahydrofuran at 20℃; [00241] 2-Methoxy-3-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)aniline (358 mg, 1 .44mmol) was completely dissolved in THF (10 mL). Water (5 mL) was added followed by sodiumperborate (569 mg, 3.7 mmol). The mixture was stirred at ambient temperature overnight. Excess THF was removed under vacuo - some solid. Saturated ammonium chloride (10mls) and DCM (50mls) were added and the mixture stirred vigourously for one hour before passing through a hydrophobic frit. The DCM was concentrated down and purified by flashchromatography eluting with 0-60% ethyl acetate/isohexane over 40 minutes. Product containing fractions were concentrated to give 3-amino-2-methoxyphenol as an off white crystalline solid, l2Smgs. [00242] 1H NMR (DMSO-d6): O 8.80 (5, 1H), 6.55 (t, J= 8.1 Hz, 1H), 6.04 (dd, J= 1.3 and 8.1 Hz, 1H), 4.71 (bs, 2H), 3.62 (5, 3H).
Same Skeleton Products
Historical Records