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229185-00-6

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229185-00-6 Usage

Description

(S S)-(-)-1-(1-NAPHTHYL)-2-(2-NAPHTHYL)& is a chiral compound that consists of two naphthyl groups connected by a single carbon. It is a stereochemically defined compound with a specific arrangement of atoms in space, resulting in two enantiomeric forms, (S)-(-) and (R)-(+), which are mirror images of each other and cannot be superimposed.

Uses

Used in Pharmaceutical Industry:
(S S)-(-)-1-(1-NAPHTHYL)-2-(2-NAPHTHYL)& is used as a chiral compound for the production of chiral pharmaceuticals and agrochemicals. Its specific arrangement of atoms in space allows for the creation of enantiomerically pure compounds, which are essential in the development of effective and safe medications.
Used in Analytical Chemistry:
(S S)-(-)-1-(1-NAPHTHYL)-2-(2-NAPHTHYL)& is used as a chiral resolving agent in chromatography. Its unique stereochemistry enables the separation of enantiomers, which is crucial in the analysis and purification of chiral compounds.
Used in Organic Synthesis:
(S S)-(-)-1-(1-NAPHTHYL)-2-(2-NAPHTHYL)& is used as a chiral auxiliary in organic synthesis. Its stereochemical properties can be exploited to control the stereoselectivity of various chemical reactions, leading to the formation of desired enantiomers with high purity.
Used in Material Science:
(S S)-(-)-1-(1-NAPHTHYL)-2-(2-NAPHTHYL)& may have potential applications in the development of new materials with specific properties based on its stereochemical arrangement. Its unique structure could be utilized to create materials with tailored properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 229185-00-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,1,8 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 229185-00:
(8*2)+(7*2)+(6*9)+(5*1)+(4*8)+(3*5)+(2*0)+(1*0)=136
136 % 10 = 6
So 229185-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H18O2/c23-21(18-13-12-15-6-1-2-8-17(15)14-18)22(24)20-11-5-9-16-7-3-4-10-19(16)20/h1-14,21-24H/t21-,22-/m0/s1

229185-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S)-1-naphthalen-1-yl-2-naphthalen-2-ylethane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1,2-Ethanediol,2-(1-naphthalenyl)-1-(2-naphthalenyl)-,(1S,2S)

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:229185-00-6 SDS

229185-00-6Downstream Products

229185-00-6Relevant articles and documents

Synthesis and Stereochemical Characterization of Some Optically Active 1,2-Dinaphthylethane-1,2-diols

Rosini, Carlo,Scamuzzi, Simone,Uccello-Barretta, Gloria,Salvadori, Piero

, p. 7395 - 7400 (1994)

Three new diols, 1,2-di(2-naphthyl)ethane-1,2-diol, 1-(1-naphthyl)-2-(2-naphthyl)ethane-1,2-diol, and 1,2-di(1-naphthyl)ethane-1,2-diol, have been prepared in optically active form by catalytic asymmetric syn-dihydroxylation of the corresponding (E)-olefins.The complete stereochemical characterization was easily accomplished by transforming them into the corresponding isopropyiidene ketals.These derivatives can be separated by HPLC on a Chiralcel OD column allowing the determination of the ee, and at same time, their CD spectra have been analyzed, allowing a safe assignment of absolute configuration in conjunction with molecular mechanics calculations and an exciton-coupling treatment.

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