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138432-99-2

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138432-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138432-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,3 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138432-99:
(8*1)+(7*3)+(6*8)+(5*4)+(4*3)+(3*2)+(2*9)+(1*9)=142
142 % 10 = 2
So 138432-99-2 is a valid CAS Registry Number.

138432-99-2Relevant articles and documents

A novel strategy for the design of smart supramolecular gels: Controlling stimuli-response properties through competitive coordination of two different metal ions

Lin, Qi,Sun, Bin,Yang, Qing-Ping,Fu, Yong-Peng,Zhu, Xin,Zhang, You-Ming,Wei, Tai-Bao

, p. 10669 - 10671 (2014)

By rationally introducing Ca2+ and Fe3+ into a supramolecular gel, a bimetal-gel CaFeG was prepared. CaFeG could reversibly "turn-on" its fluorescence upon sensing H2PO 4- with specific selectivity un

Double metal ions competitively control the guest-sensing process: A facile approach to stimuli-responsive supramolecular gels

Lin, Qi,Sun, Bin,Yang, Qing-Ping,Fu, Yong-Peng,Zhu, Xin,Wei, Tai-Bao,Zhang, You-Ming

, p. 11457 - 11462 (2014)

A facile approach to the design of stimuli-responsive supramolecular gels (SRSGs) termed double-metal-ion competitive coordination control is reported. By this means, the fluorescence signals and guest-selective responsiveness of the SRSGs are controlled

An efficient iodide ion chemosensor and a rewritable dual-channel security display material based on an ion responsive supramolecular gel

Lin, Qi,Liu, Lu,Liu, Juan,Zheng, Feng,Zhang, You-Ming,Yao, Hong,Wei, Tai-Bao

, p. 38210 - 38215 (2017)

By introducing multi-self-assembly driving forces, coordination binding sites and signal groups into the same molecule, a well designed functional gelator G1 was synthesized. The gelator G1 could form a stable Pb2+-coordinated supramolecular me

Columnar self-assembly of luminescent bent-shaped hexacatenars with a central pyridine core connected with substituted 1,3,4-oxadiazole and thiadiazoles

Pradhan, Balaram,Gupta, Ravindra Kumar,Pathak, Suraj Kumar,De, Joydip,Pal, Santanu Kumar,Achalkumar, Ammathnadu S.

, p. 3781 - 3798 (2018/03/06)

Bent-shaped molecules with a central pyridine core flanked with substituted 1,3,4-oxadiazole and thiadiazole derivatives with a variation in the number and length of terminal tails were synthesized. Thiadiazole based compounds exhibited a wider mesophase

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