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58649-05-1

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58649-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58649-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,4 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58649-05:
(7*5)+(6*8)+(5*6)+(4*4)+(3*9)+(2*0)+(1*5)=161
161 % 10 = 1
So 58649-05-1 is a valid CAS Registry Number.

58649-05-1Relevant articles and documents

Cage Like Al-KIT-5 Mesoporous Materials for C-C Bond Formation Reactions under Solvent Free Conditions

Baruah, Pranjal K.,Dutta, Prantu,Kalita, Pranjal

, p. 2037 - 2045 (2015/12/24)

The C-C bond forming reactions are of fundamental importance in chemistry. As a result there is ever growing interest for chemists to develop new methods for C-C bond formation. We report here three dimensional nano-cage mesoporous aluminosilicate materia

NO cations as highly efficient catalysts for carbon-carbon bond forming reactions

Yamashita, Yasuhiro,Kobayashi, Shue

supporting information; scheme or table, p. 678 - 679 (2011/04/22)

NO cations were found to be a highly effective catalysts in several carbon-carbon bond forming reactions. For example, [3 + 2] cycloadditions of nitrones or azomethine imines with vinyl ethers proceeded in the presence of 0.1-1 mol % of the NO cation to afford the desired adducts in high yields. Copyright

An efficient synthesis of 3,4-dihydropyran-2-one derivatives by Lewis base-catalyzed tandem Michael addition and lactonization

Tozawa, Takashi,Fujisawa, Hidehiko,Mukaiyama, Teruaki

, p. 1454 - 1455 (2007/10/03)

A convenient one-pot preparation of 3,4-dihydropyran-2-one derivatives by Michael addition of silyl enolate derived from phenyl ester with α,β-unsaturated ketones in the presence of a Lewis base catalyst such as tetrabutylammonium phenoxide was developed. In this catalytic cycle, 3,4-dihydropyran-2-ones were produced in good to excellent yields via intramolecular cyclization of in situ formed Michael-adducts.

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