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2,6-Bis[(R)-4-phenyloxazolin-2-yl]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

342043-03-2

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342043-03-2 Usage

Classification

Chiral ligand

Usage

Commonly used in asymmetric catalysis

Structure

Pyridine-based compound with two oxazoline groups and a phenyl ring attached to the nitrogen atoms

Function

Coordinates with transition metal ions to promote various asymmetric reactions, such as asymmetric hydrogenation and allylic substitution

Application

Widely used in organic synthesis to produce enantiomerically pure compounds with high selectivity and efficiency, making it a valuable tool in the field of asymmetric catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 342043-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,0,4 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 342043-03:
(8*3)+(7*4)+(6*2)+(5*0)+(4*4)+(3*3)+(2*0)+(1*3)=92
92 % 10 = 2
So 342043-03-2 is a valid CAS Registry Number.

342043-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyl-2-[6-(4-phenyl-4,5-dihydro-1,3-oxazol-2-yl)pyridin-2-yl]-4,5-dihydro-1,3-oxazole

1.2 Other means of identification

Product number -
Other names PYR313

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:342043-03-2 SDS

342043-03-2Upstream product

342043-03-2Relevant articles and documents

The rapid synthesis of oxazolines and their heterogeneous oxidation to oxazoles under flow conditions

Gl?ckner, Steffen,Tran, Duc N.,Ingham, Richard J.,Fenner, Sabine,Wilson, Zoe E.,Battilocchio, Claudio,Ley, Steven V.

supporting information, p. 207 - 214 (2015/02/02)

A rapid flow synthesis of oxazolines and their oxidation to the corresponding oxazoles is reported. The oxazolines are prepared at room temperature in a stereospecific manner, with inversion of stereochemistry, from β-hydroxy amides using Deoxo-Fluor. The

Homogeneous asymmetric hydrogenation catalyst

-

, (2009/08/18)

Provide that a useful catalyst for homogeneous hydrogenation, particularly a catalyst for homogeneous asymmetric hydrogenation for hydrogenation, particularly asymmetric hydrogenation, which is obtainable with comparative ease and is excellent in economically and workability, and a process for producing a hydrogenated compound of an unsaturated compound, particularly an optically active compound using said catalyst with a high yield and optical purity.

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