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Phenol, 2,4-dinitro-, compd. with N,N-diethylethanamine (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20399-10-4

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20399-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20399-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20399-10:
(7*2)+(6*0)+(5*3)+(4*9)+(3*9)+(2*1)+(1*0)=94
94 % 10 = 4
So 20399-10-4 is a valid CAS Registry Number.

20399-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dinitro-phenol, compound with triethylamine

1.2 Other means of identification

Product number -
Other names 2,4-Dinitro-phenol, Verbindung mit Triaethylamin

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:20399-10-4 SDS

20399-10-4Relevant academic research and scientific papers

Photo-/Baso-Chromisms and the Application of a Dual-Addressable Molecular Switch

Liu, Danyang,Yu, Binhong,Su, Xing,Wang, Xiaojun,Zhang, Yu-Mo,Li, Minjie,Zhang, Sean Xiao-An

, p. 2838 - 2845 (2019)

Two typical molecular switches of spiropyran (SP) and benzoxazine (OX) were fused by sharing an indole to achieve a new dual-addressable molecular switch (SP-OX-NO2). Through proper molecular modification with NO2, the transformation

STERIC FACTORS IN THE SHORT-RANGE SOLVATION OF SECONDARY AMINES

Tayh, Jamal A.,Scott, Ronald M.

, p. 297 - 305 (2007/10/02)

Steric aspects of the short-range solvation of proton transfer complexes between 2,4-dinitrophenol and various secondary amines was studied in benzene-DMSO and benzene-dioxane mixed solvent systems.Diisopropylamine was hindered when compared with diethylamine, and 2,2,6,6-tetramethylpiperidine was hindered when compared with 2,6-dimethylpiperidine in forming the proton transfer complex.The smaller electron-donating solvent dimethylsulfoxide was capable of solvating the more hindered amines, but the the bulkier dioxane could only solvate diethylamine and dimethylpiperidine readily.Tetrahydropyran could solvate tetramethylpiperidine weakly, inferring that it did not solvate in precisely the same fashion as does dioxane.It is concluded that the solvation structure is sufficiently crowded as to be sensitive to small changes in the structures of the participants.

Amine basicities in benzene and in water

Frenna, Vincenzo,Vivona, Nicolo,Consiglio, Giovanni,Spinelli, Domenico

, p. 1865 - 1868 (2007/10/02)

The constants for ion-pair formation with 2,4-dinitrophenol in benzene (KB), the pKa values in water, of thirty-three amines have been measured.According to the class of amine, two different situations can be observed: for primary amines and secundery cyclic amines, the effects of structural variations on basicity are higher in water than in benzene; on the other hand, for tertiary amines these effects are similar in the two solvents.KB Values of primary amines give a good correlation with ? *.The Tatf and Hancock equation allows a unifying treatment of KB values of the various classes of amines.

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