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sodium 3,5-dichlorophenolate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52214-59-2

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52214-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52214-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,1 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52214-59:
(7*5)+(6*2)+(5*2)+(4*1)+(3*4)+(2*5)+(1*9)=92
92 % 10 = 2
So 52214-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl2O.Na/c7-4-1-5(8)3-6(9)2-4;/h1-3,9H;/q;+1/p-1

52214-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,3,5-dichlorophenolate

1.2 Other means of identification

Product number -
Other names Sodium 3,5-dichlorophenolate

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:52214-59-2 SDS

52214-59-2Relevant academic research and scientific papers

Selective Heteronuclear NOE Enhancements in Benzoheterocycles. Effect of Ring Size on Indirect Three-Spin Effects

Redondo, Jordi,Sanchez-Ferrando, Francisco,Valls, Montserrat,Virgili, Albert

, p. 511 - 517 (2007/10/02)

The 80 MHz 1H NMR and 20 MHz 13C NMR spectra of five 4-methylcoumarins, six 4-methyl-2(1H)-quinolones and nine 3-methylbenzofurans, including six new compounds, were fully assigned.Homonuclear 1H NOEs and selective heteronuclear 13C NOEs were measured after low-power pre-saturation of the methyl protons.Indirect, negative heteronuclear NOE enhancements were found in suitable three-spin systems of the 13C-1H- type, and their magnitude was found to be dependent on ring size.The first examples of indirect, heteronuclear NOE enhancements on non-protonated carbons are described.KEY WORDS Heteronuclear NOE Selective heteronuclear 13C NOE Indirect negative NOE 13C-1H- three-spin effects Coumarins 2(1H)-Quinolones Benzofurans.

Mechanisms of Nucleophilic Attack at Carbon-Nitrogen Double Bonds. The Reaction of Aryl N-Arylbenzimidates with Methoxide Ion

Rowe, Jeffrey E.

, p. 1259 - 1262 (2007/10/02)

Rate data for the reaction of three series of aryl N-arylbenzimidates with methoxide ion at 303 K are presented.Linear Hammett plots were obtained for each series.Solvent isotope effects have also been measured.The results are interpreted in terms of rate-determining formation of a tetrahedral intermediate, irrespective of the nature of the substituent.

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