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28045-36-5

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28045-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28045-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,4 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28045-36:
(7*2)+(6*8)+(5*0)+(4*4)+(3*5)+(2*3)+(1*6)=105
105 % 10 = 5
So 28045-36-5 is a valid CAS Registry Number.

28045-36-5Relevant articles and documents

Thermodynamic Resolution and Enantioselective Synthesis of C2-Symmetric Bis-sulfoxides Based on Chiral Iridium(III) Complexes

Li, Li-Ping,Peng, He-Long,Ye, Bao-Hui

, p. 12245 - 12253 (2019/10/11)

Enantiopure λ-[Ir(dfppy)2(MeCN)2](PF6) and Δ-[Ir(dfppy)2(MeCN)2](PF6) (where dfppy is (4,6-difluoropheny)pyridine) were demonstrated to preferentially react with (S,S)-1,2-bis(arylsulfinyl)

A Bulky Disulfoxide Ligand for Pd-Catalyzed Oxidative Allylic C-H Amination with 2,2,2-Trichloroethyl Tosyl Carbamate

Li, You-Gui,Li, Li,Yang, Ming-Yue,He, Gang,Kantchev, Eric Assen B.

, p. 4907 - 4917 (2017/05/12)

Challenging substrates and conditions in homogeneous catalysis pose stringent demands on the ligands used. A novel, bulky, 1-adamantyl-substituted disulfoxide ligand designed after a systematic evaluation of the electronic and steric properties of disulfoxide substituents permits the allylic oxidative C-N coupling reaction to proceed at lower catalyst loading while requiring a smaller excess of reagents. Additionally, this ligand improves the yields when TsNHCOOCH2CCl3, a novel reagent that permits deprotection of the products under both acidic and basic conditions, is used.

Catalytic intermolecular allylic C-H alkylation

Young, Andrew J.,White, M. Christina

supporting information; experimental part, p. 14090 - 14091 (2009/03/11)

The first electrophilic Pd(II)-catalyzed allylic C-H alkylation is reported, providing a novel method for formation of sp3-sp3 C-C bonds directly from C-H bonds. A wide range of aromatic and heteroaromatic linear (E)-α-nitro-arylpent

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