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4,4,5,5-tetramethyl-2-(3-propylphenyl)-1,3,2-dioxaborolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1402884-05-2

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1402884-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402884-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,8,8 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1402884-05:
(9*1)+(8*4)+(7*0)+(6*2)+(5*8)+(4*8)+(3*4)+(2*0)+(1*5)=142
142 % 10 = 2
So 1402884-05-2 is a valid CAS Registry Number.

1402884-05-2Relevant academic research and scientific papers

NOVEL CELL METABOLISM MODULATING COMPOUNDS AND USES THEREOF

-

, (2021/07/31)

A class of compounds that bind to fatty acid binding protein (FABP4) and modulate adipocyte metabolism to drive enhanced glucose utilization, as well as pharmaceutical compositions comprising the class of compounds, in combination with a pharmaceutically acceptable diluent or carrier, and optionally, further in combination with a therapeutically active agent, and the use of these compounds in medicine and for the preparation of a medicament in the treatment of disorders acting on the FABP4.

Nickel-Catalyzed C(sp2)-H Borylation of Arenes

Das, Arpan,Hota, Pradip Kumar,Mandal, Swadhin K.

, p. 3286 - 3293 (2019/09/12)

In this study, C(sp2)-H borylation of arenes was accomplished by a nickel catalyst, resulting in good yield. Alkyl and alkoxy arenes were successfully functionalized, affording C(sp2)-H borylated compounds. It was unraveled that the well-defined abnormal N-heterocyclic carbene based Ni(II) complex breaks into Ni nanoparticles (Ni-NPs), which act as catalytically active species. A series of controlled reactions under stoichiometric conditions along with spectroscopic studies and single-crystal X-ray crystallographic study helped us to understand the formation of Ni-NPs along with formation of a boron(III) compound during this reaction.

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