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13842-97-2

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13842-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13842-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,4 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13842-97:
(7*1)+(6*3)+(5*8)+(4*4)+(3*2)+(2*9)+(1*7)=112
112 % 10 = 2
So 13842-97-2 is a valid CAS Registry Number.

13842-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name PENTAFLUOROPHENYL METHACRYLATE

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:13842-97-2 SDS

13842-97-2Downstream Products

13842-97-2Relevant articles and documents

Effect of the chain length of N-alkyl-β-alanine on their copper complex formation in aqueous solution

Nakamura,Koshinuma,Tajima

, p. 335 - 339 (2007/10/02)

The effects of the chain length of N-alkyl-β-alanine (NAA) (the number of carbon atoms in the alkyl chains; n=0, 2, 4, 6, 8, 10, 12) on the copper(II) complex formation and its properties were investigated. The complex formation constants for two-step reactions were determined by potentiometry using the selective electrodes of copper(II) and hydrogen ions. The values of the complex formation constants decreased with increasing chain length of the alkyl substituents, and became constant for the substituents longer than the butyl group. These results could be explained in terms of a steric hindrance effect of the N-alkyl substituents on these coordination reactions. Each logarithmic function of the solubility and of the solubility product of the 1(Cu):2(NAA)-complexes was found to be expressed, respectively, as a linear function of the number of carbon atoms in the alkyl group. From these data, the standard free energies of the formation and the precipitation of the 1:2-complexes from these constituent ions have been estimated, and a standard free energy diagram was constructed for 1:2-complex formation. It was concluded that the hydrophobic interaction is a driving force which promotes crystalline complex formation from the constituent ions.

Thermal Decomposition of Copper Complexes of Aminoacids

Eroshkin, V. I.,Shelkovnikov, V. V.,Tronov, A. B.,Durasov, V. B.

, p. 1472 - 1475 (2007/10/02)

The thermal decomposition processes of copper complexes have been examined and their fundamental characteristics determined: the temperature and rate of decomposition and the activation energy.The stability series of the compounds investigated has been set up on the basis of the results and compared with the thermodynamic characteristics of the complex formation reactions.

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