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53458-15-4

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53458-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53458-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,5 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53458-15:
(7*5)+(6*3)+(5*4)+(4*5)+(3*8)+(2*1)+(1*5)=124
124 % 10 = 4
So 53458-15-4 is a valid CAS Registry Number.

53458-15-4SDS

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 1,2-bis(4-ethoxyphenyl)-2-hydroxyethanone

1.2 Other means of identification

Product number -
Other names 4,4'-diethoxy-benzoin

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:53458-15-4 SDS

53458-15-4Downstream Products

53458-15-4Relevant articles and documents

Enantioselective reduction and deracemisation using the non-conventional yeast Pichia glucozyma in water/organic solvent biphasic systems: Preparation of (S)-1,2-diaryl-2-hydroxyethanones (benzoins)

Fragnelli, Maria Caterina,Hoyos, Pilar,Romano, Diego,Gandolfi, Raffaela,Alcántara, Andrés R.,Molinari, Francesco

experimental part, p. 523 - 528 (2012/01/13)

Water/organic solvent two-liquid-phase systems have been successfully applied in the synthesis of enantiomerically pure (S)-benzoin through two different methodologies catalysed by whole cells from the non-conventional yeast Pichia glucozyma: the stereoselective monoreduction of benzil and the deracemisation of benzoin. The presence of the organic solvent influences the redox systems implied in the reactions, avoiding the formation of the corresponding diols, increasing the enantioselectivity and allowing the easy isolation of the products in high yields and excellent enantiomeric excesses. The use of both strategies has been extended to the preparation of different chiral benzoin derivatives.

The Preparation and Measurement of the Temperatures and Heats of Transition of the Liquid Crystal Phases of Two Homologous Series: 2-hydroxy-1,2-bis(4-n-alkyloxyphenyl)-1-(4-ethoxyphenyl)iminoethane and (4-n-decyloxyphenyl)iminoethane

Bennur, S. C.,Kroin, T.,Ouriques, G. R.,Taylor, T. R.

, p. 277 - 288 (2007/10/02)

Two homologous series A and B, viz, 2-hydroxy-1,2-bis(4-n-alkyloxyphenyl)-1-(4-ethoxyphenyl) and 2-hydroxy-1,2-bis(4-n-alkyloxyphenyl)-1-(4-n-decyloxyphenyl)iminoethanes have been prepared with varying number of carbon atoms in the alkoxy chain.The transition temperatures and textures of the mesophases were determined with a polarizing microscope equipped with a Mettler FP-5 hot stage.The transition temperatures and transition heats were measured using a Perkin-Elmer DSC-2.The compounds of the two series with the same number of carbon atoms do not exhibit the same mesophases.Series A exhibits a nematic phase for compounds with n = 1-16 and also a smectic phase for compounds with n = 10, 12 and 16.Series B shows a nematic mesophase for compounds with n /= 5.

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