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16397-74-3

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16397-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16397-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,9 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16397-74:
(7*1)+(6*6)+(5*3)+(4*9)+(3*7)+(2*7)+(1*4)=133
133 % 10 = 3
So 16397-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H28O2/c1-3-5-9-13(4-2)12-17-15(16)14-10-7-6-8-11-14/h13-14H,3-12H2,1-2H3

16397-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylhexyl cyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names Cyclohexanecarboxylicacid,2-ethylhexyl ester

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:16397-74-3 SDS

16397-74-3Downstream Products

16397-74-3Relevant articles and documents

High-Pressure NMR Study of Transport and Relaxation in Complex Liquids of 2-Ethylhexyl Cyclohexanecarboxylate and 2-Ethylhexyl Benzoate

Jonas, J.,Adamy, S. T.,Grandinetti, P. J.,Masuda, Y.,Morris, S. J.,et al.

, p. 1157 - 1164 (1990)

The self-diffusion coefficients, densities, and shear viscosities of liquid 2-ethylhexyl cyclohexanecarboxylate (EHC) were measured as a function of pressure from 1 to 4500 bar within the temperature range from -20 deg C to 80 deg C.The Stokes-Einstein equation is applicable over 5 order of magnitude changes in self-diffusion and viscosity.The experimental data obtained are compared to those for the complex liquid of 2-ethylhexyl benzoate (EHB) in order to characterize the molecular structure effect of the replacement of the benzene ring with a saturated cyclohexyl ring.In particular, the low-temperature data suggest that conjugation of the phenyl ring with the ester group in EHB slows down diffusion and increases viscosity in comparison with EHC.Analysis in terms of the rough hard sphere model indicates a high degree of rotational-translational coupling which increases as density increases.By use of high-resolution, high-pressure NMR techniques the natural-abundance 13C spin-lattice relaxation times T1, and nuclear Overhauser enhancement were measured for each individual carbon in EHC and EHB over the same range of temperatures and pressures.An approximate analysis of the experimental T1 data indicates anisotropic reorientation with multiple internal rotations.

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