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1214370-35-0

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1214370-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1214370-35-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,3,7 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1214370-35:
(9*1)+(8*2)+(7*1)+(6*4)+(5*3)+(4*7)+(3*0)+(2*3)+(1*5)=110
110 % 10 = 0
So 1214370-35-0 is a valid CAS Registry Number.

1214370-35-0Downstream Products

1214370-35-0Relevant articles and documents

Regioselective Direct C-H Trifluoromethylation of Pyridine

Yang, Xiao,Sun, Rui,Li, Shun,Zheng, Xueli,Yuan, Maolin,Xu, Bin,Jiang, Weidong,Chen, Hua,Fu, Haiyan,Li, Ruixiang

, p. 7108 - 7112 (2020/10/02)

A highly efficient and regioselective direct C-H trifluoromethylation of pyridine based on an N-methylpyridine quaternary ammonium activation strategy has been developed. A variety of trifluoromethylpyridines can be obtained in good yield and excellent re

A Monophosphine Ligand Derived from Anthracene Photodimer: Synthetic Applications for Palladium-Catalyzed Coupling Reactions

Wang, Xin,Liu, Wei-Gang,Tung, Chen-Ho,Wu, Li-Zhu,Cong, Huan

, p. 8158 - 8163 (2019/09/07)

Herein, we present an air-stable dianthracenyl monophosphine ligand (diAnthPhos) which can be prepared in two steps from commercially available anthracene derivatives. The ligand exhibits excellent efficiency for palladium-catalyzed coupling reactions. In particular, Miyaura borylation of heterocycle-containing electrophiles can be facilitated employing the diAnthPhos ligand with a broad substrate scope and low catalyst loading. The valuable synthetic utility of the new ligand is further demonstrated by a one-pot Miyaura borylation/Suzuki coupling protocol for heteroaryl-containing substrates.

Borazine-CF3? Adducts for Rapid, Room Temperature, and Broad Scope Trifluoromethylation

Geri, Jacob B.,Wade Wolfe, Michael M.,Szymczak, Nathaniel K.

supporting information, p. 1381 - 1385 (2018/01/15)

A fluoroform-derived borazine CF3? transfer reagent is used to effect rapid nucleophilic reactions in the absence of additives, within minutes at 25 °C. Inorganic electrophiles spanning seven groups of the periodic table can be trifluoromethylated in high yield, including transition metals used for catalytic trifluoromethylation. Organic electrophiles included (hetero)arenes, enabling C?H and C?X trifluoromethylation reactions. Mechanistic analysis supports a dissociative mechanism for CF3? transfer, and cation modification afforded a reagent with enhanced stability.

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