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acetaldehyde dibenzylacetal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23556-90-3

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23556-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23556-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,5 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23556-90:
(7*2)+(6*3)+(5*5)+(4*5)+(3*6)+(2*9)+(1*0)=113
113 % 10 = 3
So 23556-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H18O2/c1-14(17-12-15-8-4-2-5-9-15)18-13-16-10-6-3-7-11-16/h2-11,14H,12-13H2,1H3

23556-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetaldehyde dibenzyl acetal

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:23556-90-3 SDS

23556-90-3Relevant academic research and scientific papers

A facile one-pot synthesis of symmetrical and unsymmetrical acetaldehyde acetals from primary alcohols

Guy,DiPietro

, p. 687 - 692 (2007/10/02)

Initial formation of a vinyl ether 2 by treatment of a primary alcohol 1 with ethyl vinyl ether in the presence of mercury (II) acetate followed by treatment with the same or a different alcohol in the presence of p-toluenesulfonic acid affords the symmetrical and unsymmetrical acetaldehyde acetals 3 in good overall yield. The method is easily scaled up and represents a significant improvement over currently available procedures.

Chiral Recognition in the Reaction of the Enolate derived from 5-C5H5)Fe(CO)(PPh3)COCH2OCH2Ph> with 1-Phenylethyl Bromide

Davies, Stephen G.,Middlemiss, David,Naylor, Alan,Wills, Martin

, p. 797 - 799 (2007/10/02)

Chiral recognition to the extent of 30:1 has been observed in the reaction between the homochiral iron acyl complex 5-C5H5)Fe(CO)(PPh3)COCH2OCH2Ph) and racemic 1-phenylethyl bromide.

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