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(R)-N-((S)-(2-(di-tert-butylphosphanyl)phenyl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide is a complex organic compound with a sulfinamide functional group and a chiral center. It is classified as a phosphine ligand, which is a type of molecule that can bind to metal ions. (R)-N-((S)-(2-(di-tert-butylphosphanyl)phenyl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide is composed of a tert-butylphosphanyl group, a 4-methoxyphenyl group, and a 2-methylpropane-2-sulfinylamide group. Its specific applications and properties depend on its use in various contexts within the field of chemistry.

2561513-53-7

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  • [S(R)]-N-[(S)-(4-methoxyphenyl)[2-(di-t-butylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide, 95%;2561513-53-7

    Cas No: 2561513-53-7

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2561513-53-7 Usage

Uses

Used in Coordination Chemistry:
(R)-N-((S)-(2-(di-tert-butylphosphanyl)phenyl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide is used as a ligand in coordination chemistry for forming complexes with transition metal ions. These complexes can be employed in catalytic reactions, enhancing the efficiency and selectivity of various chemical processes.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-N-((S)-(2-(di-tert-butylphosphanyl)phenyl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide is used as a reagent for chemical transformations. Its unique structure allows it to participate in a variety of reactions, contributing to the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
(R)-N-((S)-(2-(di-tert-butylphosphanyl)phenyl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide may also find applications in the pharmaceutical industry, where it could be utilized in the development of new drugs or as a key intermediate in the synthesis of bioactive compounds.
Used in Material Science:
(R)-N-((S)-(2-(di-tert-butylphosphanyl)phenyl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide may also be used in material science for the development of new materials with specific properties, such as catalysts for various industrial processes or components in advanced materials with unique characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 2561513-53-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,5,6,1,5,1 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2561513-53:
(9*2)+(8*5)+(7*6)+(6*1)+(5*5)+(4*1)+(3*3)+(2*5)+(1*3)=157
157 % 10 = 7
So 2561513-53-7 is a valid CAS Registry Number.

2561513-53-7Downstream Products

2561513-53-7Relevant articles and documents

Design and Synthesis of TY-Phos and Application in Palladium-Catalyzed Enantioselective Fluoroarylation of gem-Difluoroalkenes

Li, Zhiming,Lin, Tao-Yan,Liu, Yu,Pan, Zhangjin,Tu, Youshao,Wu, Hai-Hong,Zhang, Junliang,Zhu, Shuai

, p. 22957 - 22962 (2020)

The first example of highly enantioselective fluoroarylation of gem-difluoroalkenes with aryl halides is presented by using a new chiral sulfinamide phosphine (Sadphos) type ligand TY-Phos. N-Me-TY-Phos can be easily synthesized on a gram scale from readily available starting materials in three steps. Salient features of this work including readily available starting materials, good yields, high enantioselectivities as well as broad substrate scope make this approach very practical and attractive. Notably, the asymmetric synthesis of an analogue of a biologically active molecule is also reported.

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