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6555-30-2

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6555-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6555-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6555-30:
(6*6)+(5*5)+(4*5)+(3*5)+(2*3)+(1*0)=102
102 % 10 = 2
So 6555-30-2 is a valid CAS Registry Number.

6555-30-2Relevant articles and documents

C(sp3)-H methylation enabled by peroxide photosensitization and Ni-mediated radical coupling

Vasilopoulos, Aristidis,Krska, Shane W.,Stahl, Shannon S.

, p. 398 - 403 (2021/05/06)

The “magic methyl” effect describes the change in potency, selectivity, and/or metabolic stability of a drug candidate associated with addition of a single methyl group. We report a synthetic method that enables direct methylation of C(sp3)-H bonds in diverse drug-like molecules and pharmaceutical building blocks. Visible light-initiated triplet energy transfer promotes homolysis of the O-O bond in di-tert-butyl or dicumyl peroxide under mild conditions. The resulting alkoxyl radicals undergo divergent reactivity, either hydrogen-atom transfer from a substrate C-H bond or generation of a methyl radical via b-methyl scission. The relative rates of these steps may be tuned by varying the reaction conditions or peroxide substituents to optimize the yield of methylated product arising from nickel-mediated cross-coupling of substrate and methyl radicals.

Two-carbon ring expansion of 1-indanones via insertion of ethylene into carbon-carbon bonds

Xia, Ying,Ochi, Shusuke,Dong, Guangbin

, p. 13038 - 13042 (2019/08/26)

A rhodium-catalyzed direct insertion of ethylene into a relatively unstrained carbon-carbon bond in 1-indanones is reported, which provides a two-carbon ring expansion strategy for preparing seven-membered cyclic ketones. As many 1-indanones are commercially available and ethylene is inexpensive, this strategy simplifies synthesis of benzocycloheptenones that are valuable synthetic intermediates for bioactive compounds but challenging to prepare otherwise. In addition, the reaction is byproduct-free, redox neutral, and tolerant of a wide range of functional groups, which may have implications on unconventional strategic bond disconnections for preparing complex cyclic molecules.

ANTI-HCMV COMPOSITIONS AND METHODS

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Page/Page column 27; 28; 37; 38; 43; 44, (2016/06/06)

This document relates to compounds useful as agents for preventing or treating human cytomegalovirus (HCMV) infections.

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