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1085411-78-4

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1085411-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1085411-78-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,5,4,1 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1085411-78:
(9*1)+(8*0)+(7*8)+(6*5)+(5*4)+(4*1)+(3*1)+(2*7)+(1*8)=144
144 % 10 = 4
So 1085411-78-4 is a valid CAS Registry Number.

1085411-78-4Downstream Products

1085411-78-4Relevant articles and documents

Acetic Acid-Promoted Rhodium(III)-Catalyzed Hydroarylation of Terminal Alkynes

Duan, Chang-Lin,Liu, Xing-Yu,Tan, Yun-Xuan,Ding, Rui,Yang, Shiping,Tian, Ping,Lin, Guo-Qiang

supporting information, p. 932 - 938 (2019/05/10)

Rhodium(III)-catalyzed hydroarylation of terminal alkynes has not previously been achieved because of the inevitable oligomerization and other side reactions. Here, we report a novel Cp?Rh(III)-catalyzed hydroarylation of terminal alkynes in acetic acid as solvent to facilitate the C-H bond activation and subsequent transformations. This reaction proceeds under mild conditions, providing an effective approach to the synthesis of alkenylated heterocycles in high to excellent yields (31-99%) with a broad substrate scope (37 examples) and good functional-group compatibility. In this transformation, the loading of the alkyne can be reduced to 1.2 equivalents, which indicates the significant role of HOAc in lowering the reaction temperature and suppressing the oligomerization of the terminal alkyne. Preliminary mechanistic studies are also presented.

RuCl3-catalyzed alkenylation of aromatic C-H bonds with terminal alkynes

Cheng, Kai,Yao, Bangben,Zhao, Jinlong,Zhang, Yuhong

supporting information; experimental part, p. 5309 - 5312 (2009/06/06)

(Chemical Equation Presented) RuCl3-catalyzed regio- and/or stereoselective alkenylation reactions of a variety of arylpyridines proceeded efficiently with terminal alkynes or allylic compounds in the presence of benzoyl peroxide or benzoic acid.

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