885007-62-5 Usage
General Description
5-Nitronaphthalene-1-boronic acid is a chemical compound that belongs to the boronic acid family. It is a derivative of naphthalene and contains a nitro group and a boronic acid functional group. 5-Nitronaphthalene-1-boronic acid is commonly used in organic synthesis as a building block for creating molecules with various applications in pharmaceuticals, agrochemicals, and materials science. It is often employed in the Suzuki coupling reaction, which is a widely used method for forming carbon-carbon bonds. Additionally, 5-Nitronaphthalene-1-boronic acid has potential uses in the field of organic electronics and optoelectronics due to its ability to form stable complexes with certain organic molecules. Overall, this chemical compound plays a crucial role in the development of various valuable products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 885007-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,0,0 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 885007-62:
(8*8)+(7*8)+(6*5)+(5*0)+(4*0)+(3*7)+(2*6)+(1*2)=185
185 % 10 = 5
So 885007-62-5 is a valid CAS Registry Number.
885007-62-5Relevant articles and documents
Pentarylene- and hexarylenebis(dicarboximide)s: Near-infrared-absorbing polyaromatic dyes
Pschirer, Neil G.,Kohl, Christopher,Nolde, Fabian,Qu, Jianqiang,Muellen, Klaus
, p. 1401 - 1404 (2007/10/03)
(Figure Presented) In the red: The synthesis and optical properties of homologous ladder-type near-infrared-absorbing chromophores, namely, two pentarylenebis(dicarboximide)s (green traces; see picture) as well as a hexarylenebis(dicarboximide) (yellow trace) have been studied. A strong bathochromic shift of the absorption maximum is noted with an increasing degree of annulation as is evident from the other traces.
