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Benzeneethanol, b-(methoxymethoxy)-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113249-14-2

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113249-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113249-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,4 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113249-14:
(8*1)+(7*1)+(6*3)+(5*2)+(4*4)+(3*9)+(2*1)+(1*4)=92
92 % 10 = 2
So 113249-14-2 is a valid CAS Registry Number.

113249-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methoxymethoxy)-1,2-diphenylethanol

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:113249-14-2 SDS

113249-14-2Downstream Products

113249-14-2Relevant academic research and scientific papers

APPLICATIONS OF α-ALKOXYORGANOCUPRATE REAGENTS IN THE REGIOSPECIFIC SYNTHESIS OF CYCLIC HOMOALDOL PRODUCTS

Linderman, Russell J.,Godfrey, Alex,Horne, Kelly

, p. 495 - 506 (2007/10/02)

Cyclic homoaldol products have been prepared via conjugate addition of α-alkoxyorganocuprate reagents to enones.The reactions are regiospecific, providing the homoaldol products in good to excellent yields.The preparation of the cuprates from the α-alkoxyorganostannane precursor is described in detail.Best results were obtained with the higher order cyano cuprate reagent using in-situ trimethylsilyl chloride.

A REACTIVITY UMPOLUNG ROUTE TO CYCLIC HOMOENOLATE ALDOL PRODUCTS VIA α-ALKOXYORGANOCUPRATE CONJUGATE ADDITIONS.

Linderman, Russell J.,Godfrey, Alex,Horne, Kelly

, p. 3911 - 3914 (2007/10/02)

Substituted α-alkoxyorganocuprate reagents readily undergo conjugate addition reactions with cyclic enones to provide homoaldol products.

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