58775-15-8 Usage
Description
3,6-Di-tert-butylfluorenone, 99% is a fluorescent yellow solid with a molecular formula of C25H30O and a molecular weight of 346.5 g/mol. It is a chemical compound with a purity of 99%, making it a valuable and reliable chemical for use in a wide range of industries and scientific fields.
Uses
Used in Organic Synthesis:
3,6-Di-tert-butylfluorenone, 99% is used as a key intermediate in the development of new chemical compounds and materials. Its unique structure and properties make it a versatile building block for the synthesis of various organic compounds.
Used in Dyes and Pigments Industry:
3,6-Di-tert-butylfluorenone, 99% is used as a colorant in the manufacture of dyes and pigments. Its fluorescent properties and high purity contribute to the production of high-quality colorants for various applications.
Used in Research and Laboratory Settings:
3,6-Di-tert-butylfluorenone, 99% is used as a reagent in research and laboratory settings. Its high purity and quality make it a reliable chemical for use in scientific experiments and studies.
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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