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(Z)-5-chloro-1-methyl-3-(4-methylbenzylidene)indolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1453119-60-2

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1453119-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1453119-60-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,3,1,1 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1453119-60:
(9*1)+(8*4)+(7*5)+(6*3)+(5*1)+(4*1)+(3*9)+(2*6)+(1*0)=142
142 % 10 = 2
So 1453119-60-2 is a valid CAS Registry Number.

1453119-60-2Downstream Products

1453119-60-2Relevant academic research and scientific papers

Rhenium-catalyzed acceptorless dehydrogenative coupling via dual activation of alcohols and carbonyl compounds

Jin, Hongming,Xie, Jin,Pan, Changduo,Zhu, Zhengbo,Cheng, Yixiang,Zhu, Chengjian

, p. 2195 - 2198 (2013/10/22)

The rhenium hetaphydride complex was found to be a versatile, homogeneous catalyst for dehydrogenative functionalization of alcohol. The dehydrogenative C-C coupling of alcohols and carbonyl compounds was carried out in the absence of base and hydrogen acceptors to afford a series of α,β-unsaturated carbonyl compounds. A possible dual activation pathway was proposed by mechanistic investigations.

Palladium/copper-catalyzed oxidative C-H alkenylation/N-dealkylative carbonylation of tertiary anilines

Shi, Renyi,Lu, Lijun,Zhang, Hua,Chen, Borui,Sha, Yuchen,Liu, Chao,Lei, Aiwen

supporting information, p. 10582 - 10585 (2013/10/21)

C-H/C-N activation: The first palladium/copper-catalyzed aerobic oxidative C-H alkenylation/N-dealkylative carbonylation of tertiary anilines has been developed. Various functional groups were tolerated and acrylic ester could also be suitable substrates. This transformation provided efficient and straightforward synthesis of biologically active 3-methyleneindolin-2-one derivatives from cheap and simple substrates. Copyright

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