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N-[(1R)-2'-amino[1,1'-binaphthalen]-2-yl]-4-methyl-benzenesulfonamide is a chemical compound with the molecular formula C21H18N2O2S. It is a sulfonamide derivative featuring a binaphthyl backbone and a methyl-benzene side chain. N-[(1R)-2'-aMino[1,1'-binaphthalen]-2-yl]-4-Methyl-BenzenesulfonaMide may have potential applications in various fields such as organic synthesis, medicinal chemistry, and materials science due to its unique structure and properties. Careful handling and adherence to safety protocols are essential when working with N-[(1R)-2'-aMino[1,1'-binaphthalen]-2-yl]-4-Methyl-BenzenesulfonaMide in laboratory settings.

512170-32-0

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512170-32-0 Usage

Uses

Used in Organic Synthesis:
N-[(1R)-2'-amino[1,1'-binaphthalen]-2-yl]-4-methyl-benzenesulfonamide is used as a key intermediate in organic synthesis for the development of new chemical compounds and materials. Its unique binaphthyl backbone and sulfonamide group provide opportunities for further functionalization and the creation of novel molecules with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, N-[(1R)-2'-amino[1,1'-binaphthalen]-2-yl]-4-methyl-benzenesulfonamide is used as a potential building block for the design and synthesis of new pharmaceutical agents. Its structural features may contribute to the development of drugs with improved efficacy, selectivity, and reduced side effects.
Used in Materials Science:
N-[(1R)-2'-amino[1,1'-binaphthalen]-2-yl]-4-methyl-benzenesulfonamide is also utilized in materials science for the development of advanced materials with specific properties. Its binaphthyl backbone and sulfonamide group can be exploited to create materials with tailored characteristics for various applications, such as sensors, catalysts, or optoelectronic devices.
Used in Pharmaceutical Industry:
N-[(1R)-2'-amino[1,1'-binaphthalen]-2-yl]-4-methyl-benzenesulfonamide is used as a potential therapeutic agent in the pharmaceutical industry. Its unique structure may offer new opportunities for the treatment of various diseases and conditions, pending further research and development.
Used in Chemical Research:
In the realm of chemical research, N-[(1R)-2'-amino[1,1'-binaphthalen]-2-yl]-4-methyl-benzenesulfonamide serves as a valuable subject for studying the properties and behavior of sulfonamide derivatives and binaphthyl compounds. This can lead to a better understanding of their reactivity, stability, and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 512170-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,2,1,7 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 512170-32:
(8*5)+(7*1)+(6*2)+(5*1)+(4*7)+(3*0)+(2*3)+(1*2)=100
100 % 10 = 0
So 512170-32-0 is a valid CAS Registry Number.

512170-32-0Relevant academic research and scientific papers

Modular metal-carbon stabilized palladium nanoparticles for the catalytic hydrogenation of N-heterocycles

Zhang, Yu,Mao, Mao,Ji, Yi-Gang,Zhu, Jie,Wu, Lei

supporting information, p. 329 - 332 (2016/01/12)

We report here the first modular metal-carbon stabilized palladium nanoparticles based on binaphthyl scaffolds, which can be prepared from palladium salts and substituted binaphthyl diazonium salts in homogeneous system through direct reduction using sodium borohydride. The resulting palladium nanoparticles subjected to the electron density of modular moieties are found to be novel and efficient catalysts for the catalytic hydrogenation of N-heterocycles, affording the corresponding adducts in good to excellent yields under mild conditions.

A novel tridentate NHC-Pd(II) complex and its application in the Suzuki and Heck-type cross-coupling reactions

Chen, Tao,Gao, Jun,Shi, Min

, p. 6289 - 6294 (2007/10/03)

A novel tridentate NHC-Pd(II) complex derived from binaphthyl-2,2′-diamine (BINAM) has been synthesized and its structure has been characterized by single crystal X-ray diffraction. This NHC-Pd(II) complex was fairly effective in Suzuki and Heck-type cross-coupling reactions to give the products in good to excellent yields in most cases.

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