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2-Aminofluoren-9-on-tosylhydrazon is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53628-96-9

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53628-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53628-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,2 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53628-96:
(7*5)+(6*3)+(5*6)+(4*2)+(3*8)+(2*9)+(1*6)=139
139 % 10 = 9
So 53628-96-9 is a valid CAS Registry Number.

53628-96-9Downstream Products

53628-96-9Relevant academic research and scientific papers

Synthesis of 9-biarylfluorenes by one-pot, three-step reactions of N-tosylhydrazones, p-bromobenzeneboronic acid, and arylboronic acids

He, Jing,Zhang, Jie,Dai, Bin,Liu, Ping

, p. 268 - 273 (2019)

A one-pot, three-step reaction of N-tosylhydrazones, p-bromobenzeneboronic acid, and arylboronic acids is established for the synthesis of 9-biarylfluorenes. Sequential formation of Csp3–Csp2 bond and Csp2–Csp2

A simple and efficient synthesis of 9-arylfluorenes via metal-free reductive coupling of arylboronic acids and N-tosylhydrazones in situ

Shen, Xu,Gu, Ningning,Liu, Ping,Ma, Xiaowei,Xie, Jianwei,Liu, Yan,He, Lin,Dai, Bin

, p. 63726 - 63731 (2015/08/11)

A general, yet efficient synthesis method of 9-arylfluorenes via metal-free reductive coupling of N-tosylhydrazones and arylboronic acids has been developed. This methodology is realized by a one-pot protocol in two steps involving the preparation of N-tosylhydrazones by reacting tosylhydrazide with 9-fluorenone derivatives, followed by the reductive coupling of arylboronic acid in the presence of potassium carbonate to afford various 9-arylfluorenes analogues in moderate to excellent yields. Importantly, the catalytic system presented here enables the use of easily accessible starting materials and can be employed on a wide variety of substrates with good functional group tolerance. This protocol could also be particularly useful for the synthesis of 9-fluorenyl-substituted carbazolyl compounds.

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