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3-methyl-3-(phenylthio)indolin-2-one is a chemical compound with the molecular formula C16H13NO2S. It is a derivative of indolin-2-one, featuring a methyl group at the 3-position and a phenylthio group also at the 3-position. 3-methyl-3-(phenylthio)indolin-2-one is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure. It is characterized by its ability to form stable intermediates in chemical reactions, which can be further functionalized to produce a range of products. The compound's properties, such as its reactivity and stability, make it a valuable building block in organic synthesis and medicinal chemistry.

2406-09-9

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2406-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2406-09-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2406-09:
(6*2)+(5*4)+(4*0)+(3*6)+(2*0)+(1*9)=59
59 % 10 = 9
So 2406-09-9 is a valid CAS Registry Number.

2406-09-9Downstream Products

2406-09-9Relevant academic research and scientific papers

Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles

Cai, Yunfei,Li, Jun,Chen, Weiliang,Xie, Mingsheng,Liu, Xiaohua,Lin, Lili,Feng, Xiaoming

supporting information; experimental part, p. 2726 - 2729 (2012/07/28)

Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles has been developed via cooperative catalysis of a chiral N,N′-dioxide- Sc(OTf)3 complex and a Bronsted base. Utilizing readily available N-(phenylthio)phthalimide as the sulfur source, a wide range of optically active 3-phenylthiooxindoles were obtained in excellent yields with excellent enantioselectivities under mild reaction conditions.

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