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176245-16-2

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176245-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176245-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,2,4 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 176245-16:
(8*1)+(7*7)+(6*6)+(5*2)+(4*4)+(3*5)+(2*1)+(1*6)=142
142 % 10 = 2
So 176245-16-2 is a valid CAS Registry Number.

176245-16-2Relevant articles and documents

Multinuclear PtII Complexes: Why Three is Better Than Two to Enhance Photophysical Properties

Chakraborty, Sourav,Aliprandi, Alessandro,De Cola, Luisa

, p. 11007 - 11012 (2020)

The self-assembly of platinum complexes is a well-documented process that leads to interesting changes of the photophysical and electrochemical behavior as well as to a change in reactivity of the complexes. However, it is still not clear how many metal u

Synthesis of Novel Di Benzo spiro bis-crown-ether

Lari, Jalil,Moradgholi, Fatemeh,Vahedi, Hooshang,Massoudi, Abdolhossein

, p. 668 - 673 (2015/11/09)

This paper focuses on the synthesis of a wide variety of di benzo spiro bis-crown compounds, in good yields using di-phenols, mono tosylates of oligoethylene glycols and caesium carbonate in acetonitrile.

Rigid-Strut-Containing crown ethers and [2]catenanes for incorporation into Metal-Organic frameworks

Zhao, Yan-Li,Liu, Lihua,Zhang, Wenyu,Sue, Chi-Hau,Li, Qiaowei,Miljanic, Ognjen S.,Yaghi, Omar M.,Fraser Stoddart

experimental part, p. 13356 - 13380 (2010/06/16)

To introduce crown ethers into the struts of metal - organic frameworks (MOFs), general approaches have been developed for the syntheses of dicarboxylic acid dibenzo[30]crown-10 (DB30C10DA), dicarboxylic acid di-2,3-naphtho[30] crown-10 (DN30C10DA), dicarboxylic acid bisparaphenylene[34]crown-10 (BPP34C10DA), and dicarboxylic acid 1, 5-naphthoparaphenylene[36]crown-10 (NPP36C10DA). These novel crown ethers not only retain the characteristics of their parent crown ethers since they can 1) bind cationic guests and 2) serve as templates for making mechanically interlocked molecules (MIMs), such as catenanes and rotaxanes, but they also present coordination sites to connect with secondary building units (SBUs) in MOFs. The binding behavior of BPP34C10DA with 1,1′-dimethy 1-4, 4′-bipyridinium bis(hexafluorophosphate) (DMBP·2PF6) has been investigated by means of UV/ Vis, fluorescence, and NMR spectroscopic techniques. The crystal superstructure of the complex DMBP·2PF6C BPP34C10DA was determined by X-ray crystallography. The NPP36C10DA-based [2]catenane (H 2NPP36C10DC·CAT4PFfi) and the BPP34C10DA-based [2]catenane (H2BPP34C10DC-CAT-4PF6) were prepared in DMF at room temperature by the template-directed clipping reactions of the planarly chiral NPP36C10DA and BPP34C10DA with 1, 1′-[1,4-phenylenebis(methylene)]di4, 4′-bipyridin-l-ium bis(hexafluorophosphate) and 1,4-bis(bromomethyl) benzene, respectively. The crystal structure of the dimethyl ester (BPP34C10DE-CAT·4PF6) of the [2]catenane H 2BPP34C10DC-CAT·4PF6 was investigated by X-ray crystallography, which revealed racemic R and S isomers with planar chirality present in the crystal in a 1:1 ratio. These crown ether based struts serve as excellent organic ligands to bind with transition metal ions in the construction of MOFs: the crown ethers BPP34C10DA and NPP36C10DA in the presence of Zn(NO3)2·4H2O afforded the MOF-1001 and MOF-1002 frameworks, respectively. The crystal structures of MOF-1001 and MOF-1002 are both cubic and display Fm3m symmetry. The unit cell parameter of the metal - organic frameworks is α= 52.9345 A. Since such MOFs, containing electron-donating crown ethers are capable of docking incoming electronaccepting substrates in a stereoelectronically controlled fashion, the present work opens a new access to the preparation and application of MOFs.

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