58775-15-8 Usage
General Description
3,6-Di-tert-butylfluorenone is a chemical compound with a purity of 99%. It is a fluorescent yellow solid with a molecular formula of C25H30O and a molecular weight of 346.5 g/mol. 3,6-Di-tert-butylfluorenone, 99% is used in various applications such as in the field of organic synthesis, particularly in the development of new chemical compounds and materials. It is also used in the manufacture of dyes and pigments, and as a reagent in research and laboratory settings. 3,6-Di-tert-butylfluorenone is known for its high purity and quality, making it a valuable and reliable chemical for use in a wide range of industries and scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 58775-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,7 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58775-15:
(7*5)+(6*8)+(5*7)+(4*7)+(3*5)+(2*1)+(1*5)=168
168 % 10 = 8
So 58775-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H24O/c1-20(2,3)13-7-9-15-17(11-13)18-12-14(21(4,5)6)8-10-16(18)19(15)22/h7-12H,1-6H3
58775-15-8Relevant articles and documents
Cu(II)-Catalyzed Ligand-Free Oxidation of Diarylmethanes and Second Alcohols in Water
Wu, Jianglong,Liu, Yan,Ma, Xiaowei,Liu, Ping,Gu, Chengzhi,Dai, Bin
supporting information, p. 1391 - 139 (2017/09/30)
We developed a simple and efficient Cu(II)-catalyzed ligand-free oxidation of diarylmethanes and secondary alcohols using 70% tert-butyl hydroperoxide (TBHP) in water. A series of diarylmethanes were directly oxidized into diaryl ketones in 67%–98% yields. Additionally, various secondary alcohols were also transformed into the desired products in 48%–98% yields. Importantly, the catalytic system in the absence of any organic solvent, surfactant, or phase transfer agent, had a wide substrate scope and a high tolerance for various functional groups.
Synthesis of 3,6-di-(tert-butyl)fluorene by nickel(0) catalyzed coupling of aryl halides
Paul, Gitendra C.,Gajewski, Joseph J.
, p. 222 - 225 (2007/10/03)
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