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1,3-Dioxepin, 4,5-dihydro-5-phenyl-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

157246-90-7

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157246-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157246-90-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,2,4 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 157246-90:
(8*1)+(7*5)+(6*7)+(5*2)+(4*4)+(3*6)+(2*9)+(1*0)=147
147 % 10 = 7
So 157246-90-7 is a valid CAS Registry Number.

157246-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-4,5-dihydro-5-phenyl-1,3-dioxepin

1.2 Other means of identification

Product number -
Other names (-)-(S)-4,5-dihydro-5-phenyl-1,3-dioxepin

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:157246-90-7 SDS

157246-90-7Relevant academic research and scientific papers

Screening of a modular sugar-based phosphite-oxazoline ligand library in asymmetric Pd-catalyzed Heck reactions

Mata, Yvette,Pàmies, Oscar,Diéguez, Montserrat

, p. 3296 - 3304 (2007)

We have synthesised a library of phosphite-oxazoline ligands derived from readily available D-glucosamine. These ligands have been successfully screened in the palladium-catalysed Heck reaction of several substrates with high regio- (up to 99%) and enanti

Enantioselective heck reactions catalyzed by chiral phosphinooxazoline-palladium complexes

Loiseleur,Hayashi,Schmees,Pfaltz

, p. 1338 - 1345 (1997)

Palladium complexes with chiral phosphinooxazoline ligands are efficient catalysts for enantioselective Heck reactions with aryl or alkenyl triflates and cyclic alkenes. In the arylation and alkenylation of 1,2-dihydrofuran, cyclopentene, 2,3-dihydro-4H-p

An efficient phosphorus-containing oxazoline ligand derived from cis-2-amino-3,3-dimethyl-1-indanol: Application to the palladium-catalyzed asymmetric Heck reaction

Hashimoto, Yukihiko,Horie, Yumi,Hayashi, Minoru,Saigo, Kazuhiko

, p. 2205 - 2210 (2000)

Enantiopure 2-[2-(diphenylphosphino)phenyl]oxazoline, derived from a non-natural chiral aminoalcohol, cis-2-amino-3,3-dimethyl-1-indanol, was found to be an efficient ligand for the palladium-catalyzed asymmetric Heck reaction. Copyright (C) 2000 Elsevier

Chiral phosphite-oxazolines: A new class of ligands for asymmetric Heck reactions

Mata, Yvette,Dieguez, Montserrat,Pamies, Oscar,Claver, Carmen

, p. 5597 - 5599 (2007/10/03)

(Chemical Equation Presented) A series of phosphite-oxazoline ligands, derived from readily available D-glucosamine, have been used for the first time in the palladium-catalyzed Heck reaction of several substrates with high regio- and enantioselectivities (ee's up to 99%) and improved activities in standard conditions.

Chirale Phosphanyldihydrooxazole in der asymmetrischen Katalyse: enantioselektive Heck-Reaktionen

Loiseleur, Olivier,Meier, Peter,Pfaltz, Andreas

, p. 218 - 220 (2007/10/03)

Keywords: Asymmetrische Katalyse; Dihydrooxazole; Heck-Reaktionen; Pd-Katalysatoren; P,N-Liganden

Palladium-Catalyzed Asymmetric Arylation of 4,7-Dihydro-1,3-dioxepin. Catalytic Asymmetric Synthesis of γ-Butyrolactone Derivatives

Koga, Yuichi,Sodeoka, Mikiko,Shibasaki, Masakatsu

, p. 1227 - 1230 (2007/10/02)

The palladium-catalyzed asymmetric arylation of 4,7-dihydro-1,3-doxepin 1d has been shown to give 2d-h (up to 75percent ee), which can be readily converted to γ-butyrolactone derivatives.The important role of molecular sieves in the asymmetric Heck reacti

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