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Cyclohexaneacetic acid, sodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54668-20-1

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54668-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54668-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,6 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54668-20:
(7*5)+(6*4)+(5*6)+(4*6)+(3*8)+(2*2)+(1*0)=141
141 % 10 = 1
So 54668-20-1 is a valid CAS Registry Number.

54668-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium cyclohexylethanoate

1.2 Other means of identification

Product number -
Other names sodium cyclohexyl acetate

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:54668-20-1 SDS

54668-20-1Downstream Products

54668-20-1Relevant academic research and scientific papers

Selective hydrogenation of arenes to cyclohexanes in water catalyzed by chitin-supported ruthenium nanoparticles

Morioka, Yuna,Matsuoka, Aki,Binder, Kellie,Knappett, Benjamin R.,Wheatley, Andrew E.H.,Naka, Hiroshi

, p. 5801 - 5805 (2016)

The selective hydrogenation of aromatic compounds to cyclohexanes was found to be promoted by chitin-supported ruthenium nanoparticles (Ru/chitin) under near-neutral, aqueous conditions without the loss of C-O/C-N linkages at benzylic positions.

Effects of structure variation on solution properties of hydrotropes: Phenyl versus cyclohexyl chain tips

Hopkins Hatzopoulos, Marios,Eastoe, Julian,Dowding, Peter J.,Grillo, Isabelle,Deme, Bruno,Rogers, Sarah E.,Heenan, Richard,Dyer, Robert

experimental part, p. 9332 - 9340 (2012/09/22)

The physicochemical behavior of the phenyl-n-alkanoate (PhenCx) and cyclohexyl-n-alkanoate (CyclohexCx) series has been investigated, supporting previous work on the understanding of hydrotropes (Hopkins Hatzopoulos, M.; Eastoe, J.; Dowding, P.J.; Rogers, S. E.; Heenan, R.; Dyer, R. Langmuir2011, 27, 12346-12353). Electrical conductivity, surface tension, 1H NMR, and small-angle neutron scattering (SANS) were used to study adsorption and aggregation in terms of critical aggregation concentration (cac). The PhenCx series exhibited very similar d log(cac)/dn to n-alkylbenzoates (CnBenz), exhibiting two branches of behavior, with a common inflection point at four linear carbons, whereas the CyclohexCx series showed no break point. Electrical conductivity and 1H NMR concentration scans indicate a difference in physicochemical behavior between higher and lower homologues in both the PhenCx and CyclohexCx series. Surface tension measurements with compounds belonging to either group gave typical Gibbs adsorption profiles, having d log(cac)/dn curves consistent with limiting headgroup areas in the region of (35-55 A2) indicating monolayer formation. SANS profiles showed no evidence for aggregates below the electrical conductivity determined cac values, inferring an "on-off" mode of aggregation. Analyses of SANS profiles was consistent with charged ellipsoidal aggregates, persisting from lower through to higher homologues in both the PhenCx and CyclohexCx series.

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