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3-BENZOOXAZOL-2-YL-BENZENE-1,2-DIOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24978-46-9

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24978-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24978-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,7 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24978-46:
(7*2)+(6*4)+(5*9)+(4*7)+(3*8)+(2*4)+(1*6)=149
149 % 10 = 9
So 24978-46-9 is a valid CAS Registry Number.

24978-46-9Upstream product

24978-46-9Downstream Products

24978-46-9Relevant academic research and scientific papers

Switchable and selective detection of Zn2+ or Cd2+ in living cells based on 3′-O-substituted arrangement of benzoxazole-derived fluorescent probes

Xu, Yongqian,Xiao, Liangliang,Sun, Shiguo,Pei, Zhichao,Pei, Yuxin,Pang, Yi

, p. 7514 - 7516 (2014)

Two benzoxazole-derived ESIPT fluorescent sensors E1 and E2 show highly selective detection of Zn2+ and Cd2+, respectively, in aqueous solution and living cells. The selectivity switching from Zn 2+ to Cd2+ is a

Synthesis of vicinal diols from various arenes with a heterocyclic, amino or carboxyl group by using recombinant Escherichia coli cells expressing evolved biphenyl dioxygenase and dihydrodiol dehydrogenase genes

Misawa, Norihiko,Nakamura, Ryoko,Kagiyama, Yukiko,Ikenaga, Hiroshi,Furukawa, Kensuke,Shindo, Kazutoshi

, p. 195 - 204 (2007/10/03)

Various aromatic molecules, in which heterocycles are linked with a phenyl or benzyl group, were converted to their respective 2,3-diols (catechols) in the benzene ring by growing cell reactions using recombinant Escherichia coli, which expressed the evolved biphenyl dioxygenase [bphA (2072)] genes and the subsequent bacterial dihydrodiol dehydrogenase (bphB) gene. These vicinal diol products showed strong in vitro inhibitory activity against the lipid peroxidation induced by free radicals and strong scavenging activity towards DPPH radicals. The vicinal diols were also synthesized from ionized monocyclic aromatics incorporating an amino or carboxyl group. Graphical abstract.

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