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N-(2-(4,5-dihydrooxazol-2-yl)phenyl)-2-((4-nitrophenyl)amino)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1570135-37-3

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1570135-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1570135-37-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,0,1,3 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1570135-37:
(9*1)+(8*5)+(7*7)+(6*0)+(5*1)+(4*3)+(3*5)+(2*3)+(1*7)=143
143 % 10 = 3
So 1570135-37-3 is a valid CAS Registry Number.

1570135-37-3Relevant academic research and scientific papers

Supramolecular ensemble of PBI derivative and copper nanoparticles: A light harvesting antenna for photocatalytic C(sp2)-H functionalization

Kaur, Sandeep,Kumar, Manoj,Bhalla, Vandana

, p. 5870 - 5883 (2016)

Supramolecular aggregates of triazole-appended perylene bisimide (PBI) derivative 3 served as reactors for the generation of copper nanoparticles (CuNPs). During the reduction process, these aggregates were oxidized to triazole N-oxide species 4. Interestingly, the in situ generated CuNPs, in combination with oxidized species 4 (supramolecular ensemble 4:CuNPs), exhibited excellent photocatalytic efficiency in C(sp2)-H alkynylation and amination reactions of arenes under mild and eco-friendly conditions (inexpensive catalyst, room temperature, mixed aqueous media, aerial conditions and visible light irradiation).

Cu(II)-mediated C-H amidation and amination of arenes: Exceptional compatibility with heterocycles

Shang, Ming,Sun, Shang-Zheng,Dai, Hui-Xiong,Yu, Jin-Quan

supporting information, p. 3354 - 3357 (2014/03/21)

A Cu(OAc)2-mediated C-H amidation and amination of arenes and heteroarenes has been developed using a readily removable directing group. A wide range of sulfonamides, amides, and anilines function as amine donors in this reaction. Heterocycles present in both reactants are tolerated, making this a broadly applicable method for the synthesis of a family of inhibitors including 2-benzamidobenzoic acids and N-phenylaminobenzoates.

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