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(Z)-3-(1-oxo-1-phenylpropan-2-ylidene)indolin-2-one is a complex organic compound with the molecular formula C17H13NO2. It is a derivative of indolin-2-one, featuring a phenylpropan-2-ylidene group attached to the 3-position in the Z-configuration. (Z)-3-(1-oxo-1-phenylpropan-2-ylidene)indolin-2-one is characterized by its conjugated double bond system, which contributes to its chemical reactivity and potential applications in the synthesis of various pharmaceuticals and other organic compounds. Its structure includes a phenyl ring, an indoline nucleus, and a carbonyl group, which are key features that define its chemical properties and potential uses in research and development.

60071-76-3

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60071-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60071-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60071-76:
(7*6)+(6*0)+(5*0)+(4*7)+(3*1)+(2*7)+(1*6)=93
93 % 10 = 3
So 60071-76-3 is a valid CAS Registry Number.

60071-76-3Downstream Products

60071-76-3Relevant academic research and scientific papers

Addition-elimination of nitroalkanes to 3-phenacylideneoxindoles—direct method for the synthesis of 3-alkenylphenacylidene-oxindoles

Fu, Yu-Xuan,Hu, Shan-Shan,Li, Shao-Yi,Li, Xiao-Juan

, p. 1067 - 1075 (2019)

The first addition-elimination of nitroalkanes to 3-phenacylideneoxindoles was developed, affording the corresponding 3-alkenylphenacylidene-oxindoles with high yields.The addition-elimination mechanism of 3-phenacylideneoxindoles with nitroalkanes and re

Synthesis of (E)-3-(2-Oxo-2-arylethylidene)indolin-2-ones through Alkyne Carbonyl Metathesis and Their Stereospecific Application towards Spiro-oxindolopyrrolizidine Scaffolds

Basu, Soumyadip,Mukhopadhyay, Chhanda

, p. 1496 - 1506 (2018/04/06)

An iron-salt catalyzed, atom economic, unfamiliar type of alkyne carbonyl metathesis strategy has been developed by using isatins and acetylenes for the regioselective synthesis of (E)-3-(2-oxo-2-arylethylidene)indolin-2-one derivatives, which has been further utilized to develop a catalyst-free methodology for the synthesis of biologically active spiro-oxindolopyrrolizidine scaffolds in a highly regio- and stereospecific manner by reacting with l-proline and aldehydes. Both methods are acceptable towards various functionalities that include electron-donating and electron-accepting groups at the ortho-, meta- and para-positions. This protocol provides an environmentally friendly reaction methodology for the synthesis of a series of (1′S,2′R,3′R,7a′R)-1′,3′,5′,6′,7′,7a′-hexahydrospiro[indoline-3,2′-pyrrolizin]-2-ones.

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