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1003858-50-1

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1003858-50-1 Usage

Type of compound

Boron-containing heterocycle

Usage

Building block for pharmaceuticals and agrochemicals, potential anti-tumor and anti-cancer activity, materials science applications such as OLEDs

Fields of promise

Medicinal chemistry, materials science, scientific investigation and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1003858-50-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,8,5 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1003858-50:
(9*1)+(8*0)+(7*0)+(6*3)+(5*8)+(4*5)+(3*8)+(2*5)+(1*0)=121
121 % 10 = 1
So 1003858-50-1 is a valid CAS Registry Number.

1003858-50-1Relevant articles and documents

Neopentylglycolborylation of aryl mesylates and tosylates catalyzed by Ni-based mixed-ligand systems activated with Zn

Wilson, Daniela A.,Wilson, Christopher J.,Moldoveanu, Costel,Resmerita, Ana-Maria,Corcoran, Patrick,Hoang, Lisa M.,Rosen, Brad M.,Percec, Virgil

, p. 1800 - 1801 (2010)

(Chemical Presented) The mixed-ligand system NiCl2(dppp)/dppf is shown to be an effective catalyst for the neopentylglycolborylation of ortho-, meta-, and para-substituted electron-rich and electrondeficient aryl mesylates and tosylates. The ad

Selective Monoarylation of Aromatic Ketones and Esters via Cleavage of Aromatic Carbon-Heteroatom Bonds by Trialkylphosphine Ruthenium Catalysts

Kondo, Hikaru,Kochi, Takuya,Kakiuchi, Fumitoshi

, p. 794 - 797 (2017)

We report here the ruthenium-catalyzed selective monoarylation of aromatic ketones bearing two ortho carbon-heteroatom (O or N) bonds. Under the newly developed catalyst system consisting of RuHCl(CO)(PiPr3)2, CsF, and sty

Nickel-Catalyzed Decarbonylative Borylation and Silylation of Esters

Pu, Xinghui,Hu, Jiefeng,Zhao, Yue,Shi, Zhuangzhi

, p. 6692 - 6698 (2016)

The nickel-catalyzed direct borylation and silylation of phenolic esters has been established. The key to this highly efficient acyl C-O bond borylative and silylative cleavage depends on the appropriate choice of different ligands and additives in the pr

Transition-Metal-Free ipso-Trifluoromethylthiolation of Lithium Aryl Boronates

Shen, Feng,Zheng, Hanliang,Xue, Xiao-Song,Lu, Long,Shen, Qilong

supporting information, p. 6347 - 6351 (2019/08/20)

A transition-metal-free direct trifluoromethylthiolation of the ipso-carbon of lithium aryl boronates with trifluoromethanesulfenate under mild conditions was described. In addition, late-stage site-selective C-H borylation/trifluoromethylation and C-Cl b

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