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745809-62-5

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745809-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 745809-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,8,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 745809-62:
(8*7)+(7*4)+(6*5)+(5*8)+(4*0)+(3*9)+(2*6)+(1*2)=195
195 % 10 = 5
So 745809-62-5 is a valid CAS Registry Number.

745809-62-5Relevant articles and documents

Study on the reactivity of diarylmethane derivatives in supercritical alcohols media: Reduction of diarylmethanols and diaryl ketones to diarylmethanes using supercritical 2-propanol

Hatano, Bunpei,Kubo, Daisuke,Tagaya, Hideyuki

, p. 1304 - 1307 (2006)

We found that diarylmethanols and diaryl ketones were smoothly reduced to the corresponding diarylalkanes using supercritical 2-propanol in good yields. Furthermore, we determined the specific reaction of fluorene using supercritical methanol at high temperature.

Ligand-Free Ru-Catalyzed Direct sp3 C-H Alkylation of Fluorene Using Alcohols

Shaikh, Moseen A.,Agalave, Sandip G.,Ubale, Akash S.,Gnanaprakasam, Boopathy

, p. 2277 - 2290 (2020/02/04)

The sp3 C-H alkylation of 9H-fluorene using alcohol and a Ru catalyst via the borrowing hydrogen concept has been described. This reaction was catalyzed by the [Ru(p-cymene)Cl2]2 complex (3 mol %) and exhibited a broad reaction scope with different alcohols, allowing primary and secondary alcohols to be employed as nonhazardous and greener alkylating agents with the formation of environmentally benign water as a byproduct. A variety of 9H-fluorene underwent selective and exclusive mono-C9-alkylation with primary alcohols in good to excellent isolated yield (26 examples, 50-92% yield), whereas this reaction with secondary alcohols in the absence of any external oxidants furnished the tetrasubstituted alkene as the major product. Furthermore, a base-mediated C-H hydroxylation of the synthesized 9H-fluorene derivatives afforded 9H-hydroxy-functionalized quaternary fluorene derivatives in excellent yield.

Nickel-catalyzed synthesis of 9-monoalkylated fluorenes from 9-fluorenone hydrazone and alcohols

Fan, Jiang-Tao,Fan, Xin-Heng,Chen, Yong-Jie,Gao, Cai-Yan,Yang, Lian-Ming

, p. 2895 - 2902 (2019/08/12)

A practical protocol was disclosed for the nickel-catalyzed C-alkylation of 9-fluorenone hydrazone with alcohols using t-BuOK as the base, and 9-monoalkylated fluorene derivatives were obtained in good yields under the benign conditions.

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