871231-48-0 Usage
Uses
Used in Pharmaceutical Research:
(R)-(-)-1,1'-BI-2-NAPHTHYL DIMETHANESUL is used as a chiral auxiliary reagent for controlling the stereochemistry of various reactions, which is crucial for the synthesis of enantiomerically pure compounds. This is important in the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Research:
(R)-(-)-1,1'-BI-2-NAPHTHYL DIMETHANESUL is used as a chiral auxiliary reagent in the synthesis of enantiomerically pure agrochemicals, which can lead to more effective and environmentally friendly pesticides and other agricultural products.
Used in Material Science Research:
(R)-(-)-1,1'-BI-2-NAPHTHYL DIMETHANESUL is used as a chiral auxiliary reagent for the development of novel materials with specific properties, such as optical activity or chiral selectivity, which can be applied in various industries.
Used in Catalyst Development:
(R)-(-)-1,1'-BI-2-NAPHTHYL DIMETHANESUL is used as a building block in the development of new catalysts with unique chiral architectures, which can improve the efficiency and selectivity of chemical reactions in various applications.
Used in Functional Material Development:
(R)-(-)-1,1'-BI-2-NAPHTHYL DIMETHANESUL is used as a key component in the synthesis of functional materials with specific chiral properties, which can be applied in areas such as sensors, separation technologies, and chiral recognition.
Check Digit Verification of cas no
The CAS Registry Mumber 871231-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,2,3 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 871231-48:
(8*8)+(7*7)+(6*1)+(5*2)+(4*3)+(3*1)+(2*4)+(1*8)=160
160 % 10 = 0
So 871231-48-0 is a valid CAS Registry Number.
871231-48-0Relevant academic research and scientific papers
Yu, Jeongjae,Armstrong, Daniel W.,Ryoo, Jae Jeong
, p. 74 - 84 (2018)
We recently reported a new C3-symmetric (R)-phenylglycinol N-1,3,5-benzenetricarboxylic acid-derived chiral high-performance liquid chromatography (HPLC) stationary phase (CSP 1) that demonstrated better results as compared to a previously described N-3,5-dintrobenzoyl (DNB) (R)-phenylglycinol-derived CSP. Over a decade ago, (S)-leucinol, (R)-phenylglycine, and (S)-leucine derivatives were used as the starting materials of 3,5-DNB-based Pirkle-type CSPs for chiral separation. In this study, three new C3-symmetric CSPs (CSP 2, 3, and 4) were prepared by combining the ideas and results mentioned above. Here we describe the synthetic procedures and applications of the new C3-symmetric CSPs (CSP 2–CSP 4).
