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1-(4-Cl-C6H4)-1,2-C2HB10H10 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23754-24-7

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23754-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23754-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,5 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23754-24:
(7*2)+(6*3)+(5*7)+(4*5)+(3*4)+(2*2)+(1*4)=107
107 % 10 = 7
So 23754-24-7 is a valid CAS Registry Number.

23754-24-7Downstream Products

23754-24-7Relevant academic research and scientific papers

Palladium-Catalyzed Direct Cross-Coupling of Carboranyllithium with (Hetero)Aryl Halides

Lu, Ju-You,Wan, Hong,Zhang, Jianwei,Wang, Zhixuan,Li, Yang,Du, Yongmei,Li, Chunying,Liu, Zhao-Tie,Liu, Zhong-Wen,Lu, Jian

, p. 17542 - 17546 (2016)

A palladium-catalyzed direct C-arylation reaction of readily available cage carboranyllithium reagents with aryl halides has been developed for the first time. This method is applicable to a wide range of aryl halide substrates including aryl iodides, aryl bromides, and heteroaromatic halides.

Light-promoted copper-catalyzed cage C-Arylation of: O-carboranes: facile synthesis of 1-Aryl-o-carboranes and o-carborane-fused cyclics

Lu, Zhenpin,Ni, Hangcheng,Xie, Zuowei

supporting information, p. 14944 - 14948 (2021/09/04)

Light-promoted, copper catalyzed cage C-H arylation of o-carboranes with aryl halides has been achieved, leading to the facile synthesis of a variety of 1-Aryl-o-carboranes and o-carborane-fused cyclics. This method has the following features: (1) using o

Nickel-catalyzed cross-coupling reactions of o-carboranyl with aryl iodides: Facile synthesis of 1-aryl-o-carboranes and 1,2-diaryl-o-carboranes

Tang, Cen,Xie, Zuowei

supporting information, p. 7662 - 7665 (2015/06/25)

A nickel-catalyzed arylation at the carbon center of o-carborane cages has been developed, thus leading to the preparation of a series of 1-aryl-o-carboranes and 1,2-diaryl-o-carboranes in high yields upon isolation. This method represents the first examp

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