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Chemical Structure| 41177-72-4 Chemical Structure| 41177-72-4

Structure of 41177-72-4

Chemical Structure| 41177-72-4

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Product Details of [ 41177-72-4 ]

CAS No. :41177-72-4
Formula : C9H7BrO3
M.W : 243.05
SMILES Code : OC(=O)C1=C2OCCC2=CC(Br)=C1
MDL No. :MFCD00191391

Safety of [ 41177-72-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H412
Precautionary Statements:P273

Application In Synthesis of [ 41177-72-4 ]

* 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 [ 41177-72-4 ]

[ 41177-72-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 35700-40-4 ]
  • [ 41177-72-4 ]
YieldReaction ConditionsOperation in experiment
0.24 g (50.3%) With bromine; iron; In acetic acid; b. Preparation of 5-bromo-2,3-dihydrobenzo[b]furan-7-carboxylic acid (15b) To an ice-cooled acetic acid solution (5 ml) of 2,3-dihydrobenzo[b]furan-7-carboxylic acid (15a) (0.33 g, 2.0 mmol) there was added iron (8 mg, 0.14 mmol) and bromine (0.32 g, 2.0 mmol) in 1 ml of acetic acid. The mixture was stirred at room temperature for 18 hours and then poured into water (20 ml). After cooling in the freezer for 11/2 hours the product was collected on a filter, and recrystallized from ethyl acetate to give 0.24 g (50.3%) of 15b as a white crystalline solid, mp 228-229 C.
0.24 g (50.3%) With bromine; iron; In acetic acid; b. Preparation of 5-bromo-2,3-dihydrobenzo[b]furan-7-carboxylic acid (15b) To an ice-cooled acetic acid solution (5 ml) of 2,3-dihydrobenzo[b]furan-7-carboxylic acid (15a) (0.33 g, 2.0 mmol) there was added iron (8 mg, 0.14 mmol) and bromine (0.32 g, 2.0 mmol) in 1 ml of acetic acid. The mixture was stirred at room temperature for 18 hours and then poured into water (20 ml). After cooling in the freezer for 1 1/2 hours the product was collected on a filter, and recrystallized from ethyl acetate to give 0.24 g (50.3%) of 15b as a white crystalline solid, mp 228-229C.
  • 2
  • [ 41177-72-4 ]
  • [ 89830-98-8 ]
  • C15H14N2O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
200 mg With potassium phosphate; copper(l) iodide; tetrabutylammomium bromide; 1,10-phenanthroline-4,7-diol; In water; at 100℃;Inert atmosphere; [0304] A mixture of Example 3j (600 mg, 2.4 mmol) and Example 3i (400 mg, 3.6 mmol), Cul (45 mg, 0.24 mmol), K3P04 (1 g, 4.8 mmol), 4,7-Dihydroxy-l, 10-phenanthroline(9 mg, 0.48 mmol), TBAB (386 mg, 1.2 mmol) in H20 (10 mL) under N2 was heated at 100°C overnight. After cooling, the reaction mixture was filtered and concentrated under reduced pressure to give the crude and further purified by silica chromatography to give the product 200 mg as yellow solid.
  • 3
  • [ 41177-72-4 ]
  • [ 89830-98-8 ]
  • C15H14N2O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
200 mg With potassium phosphate; copper(l) iodide; tetrabutylammomium bromide; 1,10-phenanthroline-4,7-diol; In water; at 100℃;Inert atmosphere; [0345] A mixture of Example 13a (600 mg, 5.55mmol) and Example 13b (400 mg, 1.65 mmol) Cul (45 mg, 0.24 mmol), K3P04 (1 g, 4.7 mmol), 4,7-Dihydroxy-l,10-phenanthroline (cas: 3922-40-5, 90 mg, 0.42 mmol), TBAB (386 mg, 1.2 mmol) in H20 (10 mL) under N2 was heated at 100 oC overnight. After cooling, filtered and concentrated under reduced pressure to give the crude and further purified by silica gelchromatography to give the product 200 mg as yellow solid. LCMS [M+1] + =271.0
 

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