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(S)-(+)-1,1'-BI-2-NAPHTHYL DIMETHANESULFONATE, with the molecular formula C26H20O2S, is a chiral molecule consisting of two naphthalene rings connected by a sulfur atom. It is known for its unique structural and electronic properties, which make it a versatile compound in various applications.

871231-47-9

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871231-47-9 Usage

Uses

Used in Organic Synthesis:
(S)-(+)-1,1'-BI-2-NAPHTHYL DIMETHANESULFONATE is used as a chiral auxiliary in the field of organic synthesis. It aids in inducing asymmetric induction during chemical reactions, which is crucial for the production of enantiomerically pure compounds. This application is particularly important in the pharmaceutical industry, where the desired biological activity is often associated with a specific enantiomer.
Used in Coordination Chemistry:
In coordination chemistry, (S)-(+)-1,1'-BI-2-NAPHTHYL DIMETHANESULFONATE acts as a ligand, forming complexes with various metal ions. These complexes can exhibit unique properties, such as catalytic activity or specific binding affinities, which can be exploited in various chemical processes and analytical techniques.
Used in Fluorescence Sensing:
Due to its electronic properties, (S)-(+)-1,1'-BI-2-NAPHTHYL DIMETHANESULFONATE has been studied for its potential applications in fluorescence sensing. It can be used to develop sensors for detecting specific analytes, such as metal ions or organic molecules, by exploiting the changes in its fluorescence properties upon interaction with the target molecule.
Used in Organic Electronics:
The unique structural and electronic properties of (S)-(+)-1,1'-BI-2-NAPHTHYL DIMETHANESULFONATE also make it a promising candidate for applications in organic electronics. It can be used in the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs), where its properties can contribute to improved device performance and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 871231-47-9 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 871231-47:
(8*8)+(7*7)+(6*1)+(5*2)+(4*3)+(3*1)+(2*4)+(1*7)=159
159 % 10 = 9
So 871231-47-9 is a valid CAS Registry Number.

871231-47-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H55249)  (S)-(+)-1,1'-Bi(2-naphthyl) dimethanesulfonate, 97%   

  • 871231-47-9

  • 250mg

  • 812.0CNY

  • Detail
  • Alfa Aesar

  • (H55249)  (S)-(+)-1,1'-Bi(2-naphthyl) dimethanesulfonate, 97%   

  • 871231-47-9

  • 1g

  • 2274.0CNY

  • Detail
  • Aldrich

  • (631787)  (S)-(+)-1,1′-Bi-2-naphthyldimethanesulfonate  97%

  • 871231-47-9

  • 631787-250MG

  • 772.20CNY

  • Detail

871231-47-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(1-methylsulfonyloxynaphthalen-2-yl)naphthalen-1-yl] methanesulfonate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:871231-47-9 SDS

871231-47-9Downstream Products

871231-47-9Relevant academic research and scientific papers

Synthesis of new C3 symmetric amino acid- and aminoalcohol-containing chiral stationary phases and application to HPLC enantioseparations

Yu, Jeongjae,Armstrong, Daniel W.,Ryoo, Jae Jeong

, p. 74 - 84 (2017/12/26)

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).

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