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[ CAS No. 3199-61-9 ]

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Cat. No.: {[proInfo.prAm]}
2D
Chemical Structure| 3199-61-9
Chemical Structure| 3199-61-9
Structure of 3199-61-9 *Storage: {[proInfo.prStorage]}

Quality Control of [ 3199-61-9 ]

Related Doc. of [ 3199-61-9 ]

SDS

Product Details of [ 3199-61-9 ]

CAS No. :3199-61-9MDL No. :MFCD03094950
Formula : C11H10O3 Boiling Point : 274°C at 760 mmHg
Linear Structure Formula :-InChI Key :-
M.W :190.20Pubchem ID :641368
Synonyms :

Computed Properties of [ 3199-61-9 ]

TPSA : 39.4 H-Bond Acceptor Count : 3
XLogP3 : - H-Bond Donor Count : 0
SP3 : 0.18 Rotatable Bond Count : 3

Safety of [ 3199-61-9 ]

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

Application In Synthesis of [ 3199-61-9 ]

  • Downstream synthetic route of [ 3199-61-9 ]

[ 3199-61-9 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 41873-61-4 ]
  • [ 3199-61-9 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 120℃; for 3h; General procedure: Compound 2a-2q(1 mmol) and K2CO3 (3 mmol) were suspended in DMF (10 mL), and the reaction mixture was warmed upto 120 C and refluxed for 3h, and then cooled to room temperature. The precipitation was separated out and purified by recrystallization to get the products 3a-3q.
  • 2
  • [ 89-95-2 ]
  • [ 105-36-2 ]
  • [ 3199-61-9 ]
  • 3
  • [ 3199-61-9 ]
  • [ 55038-01-2 ]
YieldReaction ConditionsOperation in experiment
With diisobutylaluminium hydride; Reference Example 28 Preparation of 2-hydroxymethylbenzofuran The reaction of 2-ethoxycarbonylbenzofurane (27.40 g) with diisobutylaluminum hydride was carried out in the manner similar to that described in Reference Example 3 to give the titled compound (16.91 g) as a colorless oil. This compound was used without further purification. 1H-NMR(CDCl3) delta: 4.76 (2H, s), 6.65 (1H, s), 7.15-7.34 (2H, m), 7.40-7.63 (2H, m). IR(KBr): 3299, 1605, 1454, 1254, 1009, 752 cm-1.
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0℃; for 0.333333h; LiAlH4 (0.19 g, 5.0 mmol) was weighed into a flask, THF (20.0 mL) was added,After stirring at 0 C for 10 minutes, 1-a (0.95 g, 5.0 mmol) was added and the mixture was stirred at 0 C for 20 minutes.The reaction was quenched by the addition of H2O (5 mL), diluted with ethyl acetate, filtered, washed with ethyl acetate,Steamed and concentrated by silica gel column chromatography to give the product as shown.
  • 5
  • [ 74225-91-5 ]
  • [ 3199-61-9 ]
  • [ 43119-53-5 ]
  • 6
  • [ 95-48-7 ]
  • [ 3199-61-9 ]
  • [ 43119-53-5 ]
  • 8
  • [ 3199-61-9 ]
  • (R)-1-(5,8-dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-en-1-yl benzofuran-2-carboxylate [ No CAS ]
  • 9
  • [ 3199-61-9 ]
  • N-(3-((6-chloro-1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)-benzofuran-2-carboxamide [ No CAS ]
  • 10
  • [ 3199-61-9 ]
  • N-(4-((1,2,3,4-tetrahydroacridin-9-yl)amino)butyl)benzofuran-2-carboxamide [ No CAS ]
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