51135-38-7

  • Product Name:7-benzoyl-2-oxindole
  • Molecular Formula:C15H11NO2
  • Purity:99%
  • Molecular Weight:237.258
InquiryAdd to cart

Product Details;

CasNo: 51135-38-7

Molecular Formula: C15H11NO2

Factory Sells Best Quality 7-benzoyl-2-oxindole 51135-38-7 with stock

  • Molecular Formula:C15H11NO2
  • Molecular Weight:237.258
  • Vapor Pressure:3.39E-10mmHg at 25°C 
  • Melting Point:154℃ 
  • Refractive Index:1.627 
  • Boiling Point:501.7 °C at 760 mmHg 
  • PKA:13.42±0.20(Predicted) 
  • Flash Point:214.3 °C 
  • PSA:46.17000 
  • Density:1.254 g/cm3 
  • LogP:2.55020 

7-BENZOYL-1,3-DIHYDRO-INDOL-2-ONE(Cas 51135-38-7) Usage

InChI:InChI=1/C15H11NO2/c17-13-9-11-7-4-8-12(14(11)16-13)15(18)10-5-2-1-3-6-10/h1-8H,9H2,(H,16,17)

51135-38-7 Relevant articles

Conformational and crystal energetics of a polymorphic cyclized product of Napafenac: The Z′ and crystal stability correlation

Nanubolu, Jagadeesh Babu,Ravikumar, Krishnan,Sridhar, Balasubramanian,Sreedhar, Bojja

, p. 133 - 145 (2014)

We report the single crystal diffraction...

Preparation method of 7-benzoyl-1,3-indoline-2-ketone

-

Paragraph 0031; 0032, (2016/11/14)

The invention discloses a preparation me...

Palladium-catalyzed direct addition of arylboronic acids to 2-aminobenzonitrile derivatives: Synthesis, biological evaluation and in silico analysis of 2-aminobenzophenones, 7-benzoyl-2-oxoindolines, and 7-benzoylindoles

Chen, Jiuxi,Ye, Leping,Su, Weike

supporting information, p. 8204 - 8211 (2015/01/08)

A palladium-catalyzed direct addition of...

Antiinflammatory agents. 3. Synthesis and pharmacological evaluation of 2-amino-3-benzoylphenylacetic acid and analogues

Walsh,Moran,Shamblee,Uwaydah,Welstead Jr.,Sancilio,Dannenburg

, p. 1379 - 1388 (2007/10/02)

A series of substituted derivatives of 2...

51135-38-7 Process route

nepafenac
78281-72-8

nepafenac

7-benzoyl-1,3-dihydroindol-2-one
51135-38-7

7-benzoyl-1,3-dihydroindol-2-one

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; water; at 30 ℃; for 3h; Temperature; Reagent/catalyst; Solvent;
92.1%
With hydrogenchloride; In ethanol; Heating;
2-oxoindoline-7-carbonitrile
380427-40-7

2-oxoindoline-7-carbonitrile

phenylboronic acid
98-80-6

phenylboronic acid

7-benzoyl-1,3-dihydroindol-2-one
51135-38-7

7-benzoyl-1,3-dihydroindol-2-one

Conditions
Conditions Yield
With 5,5'-dimethyl-2,2'-bipyridine; methanesulfonic acid; palladium(II) trifluoroacetate; water; In 2-methyltetrahydrofuran; at 80 ℃; for 36h; Schlenk technique;
89%

51135-38-7 Upstream products

  • 50-00-0
    50-00-0

    formaldehyd

  • 61941-57-9
    61941-57-9

    2-amino-3-benzoylbenzeneacetic acid,ethyl ester

  • 61085-33-4
    61085-33-4

    7-benzoyl-3-methylsulfanyl-1,3-dihydro-indol-2-one

  • 76049-81-5
    76049-81-5

    3-chloro-7-benzoylindole

51135-38-7 Downstream products

  • 51579-82-9
    51579-82-9

    amfenac

  • 104039-30-7
    104039-30-7

    Ethyl 7-benzoyloxindole-3-carboxylate

  • 61941-56-8
    61941-56-8

    2-amino-3-benzoylbenzeneacetic acid,sodium salt

Relevant Products

Shopping Cart

Clear Inquiry