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88-87-9

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88-87-9 Usage

General Description

4-Chloro-2,6-dinitrophenol, also known as DCP or 2,6-dinitro-4-chlorophenol, is a highly toxic and potentially lethal chemical compound. It is primarily used as a pesticide and wood preservative, but also has a history of being used as a weight loss aid due to its ability to increase metabolism and burn fat. However, it is not approved for human consumption and has been banned for such use by various regulatory agencies due to its inherent dangers. Exposure to 4-Chloro-2,6-dinitrophenol can lead to symptoms such as nausea, vomiting, abdominal pain, dizziness, and in severe cases, even death. Its extreme toxicity and potential for misuse make it a highly regulated and controlled substance.

Check Digit Verification of cas no

The CAS Registry Mumber 88-87-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88-87:
(4*8)+(3*8)+(2*8)+(1*7)=79
79 % 10 = 9
So 88-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClN2O5/c7-3-1-4(8(11)12)6(10)5(2-3)9(13)14/h1-2,10H

88-87-9SDS

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 4-CHLORO-2,6-DINITROPHENOL

1.2 Other means of identification

Product number -
Other names 4-chloro-2,6-dinitro-phenol

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:88-87-9 SDS

88-87-9Relevant articles and documents

Semiquinone-bridged bisdithiazolyl radicals as neutral radical conductors

Yu, Xin,Mailman, Aaron,Lekin, Kristina,Assoud, Abdeljalil,Robertson, Craig M.,Noll, Bruce C.,Campana, Charles F.,Howard, Judith A. K.,Dube, Paul A.,Oakley, Richard T.

, p. 2264 - 2275 (2012)

Semiquinone-bridged bisdithiazolyls 3 represent a new class of resonance-stabilized neutral radical for use in the design of single-component conductive materials. As such, they display electrochemical cell potentials lower than those of related pyridine-bridged bisdithiazolyls, a finding which heralds a reduced on-site Coulomb repulsion U. Crystallographic characterization of the chloro-substituted derivative 3a and its acetonitrile solvate 3a·MeCN, both of which crystallize in the polar orthorhombic space group Pna21, revealed the importance of intermolecular oxygen-to-sulfur (CO...SN) interactions in generating rigid, tightly packed radical π-stacks, including the structural motif found for 3a·MeCN in which radicals in neighboring π-stacks are locked into slipped-ribbon-like arrays. This architecture gives rise to strong intra- and interstack overlap and hence a large electronic bandwidth W. Variable-temperature conductivity measurements on 3a and 3a·MeCN indicated high values of θ(300 K) (>10 -3 S cm-1) with correspondingly low thermal activation energies Eact, reaching 0.11 eV in the case of 3a·MeCN. Overall, the strong performance of these materials as f = 1/ 2 conductors is attributed to a combination of low U and large W. Variable-temperature magnetic susceptibility measurements were performed on both 3a and 3a·MeCN. The unsolvated material 3a orders as a spin-canted antiferromagnet at 8 K, with a canting angle φ = 0.14° and a coercive field Hc = 80 Oe at 2 K.

Visible-Light-Induced Radical Polynitration of Arylboronic Acids: Synthesis of Polynitrophenols

Zhang, Qi,Raveendra Babu, Kaki,Huang, Zhouliang,Song, Jinna,Bi, Xihe

supporting information, p. 2891 - 2896 (2018/06/20)

We report a visible light-assisted one-pot method for the synthesis of polynitrophenols through radical tandem hydroxylation and nitration of arylboronic acids by utilizing copper(II) nitrate tri-nitydrate as the nitro source. This method features mild conditions, a simple procedure, and good functional group tolerance. Compared to conventional methods, this work provides a straightforward approach for the polynitration of aromatic compounds.

Nitration of phenolic compounds by antimony nitrate

Jirandehi, Hassan Fathinejad,Mirzaeian, Marjan

experimental part, p. 284 - 286 (2011/07/08)

Antimony nitrate is new compound to be an efficient nitration reagent in the nitration of phenolic compounds with high yields. This producerworks efficiently onmost of the examples, as a grinding nitration reaction, proceed very fast (~1 min) and thermogenic. Copyright Taylor & Francis Group, LLC.

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