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1415328-91-4

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1415328-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415328-91-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,3,2 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1415328-91:
(9*1)+(8*4)+(7*1)+(6*5)+(5*3)+(4*2)+(3*8)+(2*9)+(1*1)=144
144 % 10 = 4
So 1415328-91-4 is a valid CAS Registry Number.

1415328-91-4Relevant articles and documents

Synergistic Effect of Squaric Acid in Bromine-Catalyzed Deoxygenation of Sulfonyl Derivatives: Mechanistic Investigations and Synthetic Applications in Electrophilic (Fluoroalkyl)sulfenylation

Xiang, Haonan,Liu, Jie,Wang, Jieping,Jiang, Lvqi,Yi, Wenbin

supporting information, p. 181 - 185 (2021/12/17)

A method for electrophilic (fluoroalkyl)sulfenylation of nucleophiles by collaborative CTAB- and squaric acid-promoted deoxygenation of sulfonyl derivatives is reported. Mechanistic studies indicate that squaric acid dramatically decreased the energy barr

Thioether aromatic heterocyclic compound and preparation method and application thereof

-

Paragraph 0051-0054, (2021/10/05)

The invention discloses a thioether aromatic heterocyclic compound and a preparation method and application thereof, and the preparation method comprises the following steps: (I) an aromatic heterocyclic compound. The thiophenol (II) and oxidizing agent i

Photocatalytic Oxidative C-H Thiolation: Synthesis of Benzothiazoles and Sulfenylated Indoles

Aceves, Ernesto Millan,Albright, Samuel T.,Cedano, Mario R.,Dinh, Andrew N.,Gustafson, Jeffrey L.,Nguyen, Ashley D.,Smith, Diane K.

, p. 1648 - 1655 (2019/08/26)

We report studies on the photocatalytic formation of C-S bonds to form benzothiazoles via an intramolecular cyclization and sulfenylated indoles via an intermolecular reaction. Cyclic voltammetry (CV) and density functional theory studies suggest that benzothiazole formation proceeds via a mechanism that involves an electrophilic sulfur radical, while the indole sulfenylation likely proceeds via a nucleophilic sulfur radical adding into a radical cationic indole. These conditions were successfully extended to several thiobenzamides and indole substrates.

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