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(S)-2'-Methoxy-[1,1']binaphthalenyl-2-ol, commonly known as (S)-BINOL, is a chiral binaphthol compound with the chemical formula C20H16O2. It is characterized by its unique structure, featuring two naphthalene rings connected by an oxygen atom, and a methoxy group at the 2' position. This chiral compound plays a significant role in asymmetric synthesis, serving as a chiral ligand in metal-catalyzed processes. Its versatile applications in organic synthesis, pharmaceuticals, agrochemicals, and fine chemicals make it a valuable building block in the chemical industry.

35193-69-2

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35193-69-2 Usage

Uses

Used in Asymmetric Synthesis:
(S)-BINOL is used as a chiral ligand in asymmetric synthesis for its ability to induce enantioselectivity in metal-catalyzed reactions. This application is crucial for the production of enantiomerically pure compounds, which are essential in various industries, including pharmaceuticals and agrochemicals.
Used in Organic Synthesis:
(S)-BINOL serves as a chiral auxiliary in organic synthesis, aiding in the preparation of various chiral compounds. Its unique structure and properties make it an ideal candidate for the synthesis of complex organic molecules with specific stereochemistry.
Used in Pharmaceutical Industry:
(S)-BINOL is used as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs with improved efficacy and selectivity. Its chiral nature allows for the creation of enantiomerically pure drug candidates, which is vital for minimizing side effects and enhancing therapeutic outcomes.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-BINOL is utilized as a precursor for the synthesis of chiral pesticides and herbicides. Its ability to induce enantioselectivity in chemical reactions ensures the production of enantiomerically pure active ingredients, leading to more effective and environmentally friendly agrochemicals.
Used in Fine Chemicals Industry:
(S)-BINOL is employed as a key intermediate in the synthesis of various fine chemicals, including fragrances, dyes, and specialty chemicals. Its unique properties and versatility make it a valuable component in the development of high-quality and high-performance products in this industry.

Check Digit Verification of cas no

The CAS Registry Mumber 35193-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,9 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35193-69:
(7*3)+(6*5)+(5*1)+(4*9)+(3*3)+(2*6)+(1*9)=122
122 % 10 = 2
So 35193-69-2 is a valid CAS Registry Number.

35193-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2'-Methoxy-[1,1']binaphthalenyl-2-ol

1.2 Other means of identification

Product number -
Other names (-)-2'-methoxy-2-hydroxy-1,1'-binaphthyl

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:35193-69-2 SDS

35193-69-2Downstream Products

35193-69-2Relevant academic research and scientific papers

Preparative Resolution of Racemates on a Chiral Liquid Chromatography Column

Pirkle, William H.,Finn, John M.

, p. 4037 - 4040 (2007/10/02)

A 2 in. x 30 in. liquid chromatography column packed with a chiral stationary phase derived from (R)-phenylglycine has been found capable of resolving gram or larger samples of a variety of racemates.Nine such resolutions are presented.The racemates resol

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