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Pentachlorophenyl acrylate is a chemical compound with the formula C9H3Cl5O2. It is derived from pentachlorophenol, a widely used pesticide and wood preservative, and acrylate, a functional group found in acrylic polymers. PENTACHLOROPHENYL ACRYLATE is characterized by its high reactivity and potential toxicity, as it combines the properties of both pentachlorophenol and acrylate. Due to its chemical structure, pentachlorophenyl acrylate can be used in various applications, such as in the synthesis of polymers and as a chemical intermediate. However, it is essential to handle PENTACHLOROPHENYL ACRYLATE with caution, as it may pose health and environmental risks due to its toxic nature.

4513-43-3

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4513-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4513-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4513-43:
(6*4)+(5*5)+(4*1)+(3*3)+(2*4)+(1*3)=73
73 % 10 = 3
So 4513-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H3Cl5O2/c1-2-3(15)16-9-7(13)5(11)4(10)6(12)8(9)14/h2H,1H2

4513-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentachlorophenyl) prop-2-enoate

1.2 Other means of identification

Product number -
Other names Acrylsaeure-pentachlorphenylester

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:4513-43-3 SDS

4513-43-3Downstream Products

4513-43-3Relevant academic research and scientific papers

Solvent-resistant antibacterial microfibers of self-quaternized block copolymers from atom transfer radical polymerization and electrospinning

Guo-Dong, Fu,Fang, Yao,Zhigang, Li,Xinsong, Li

, p. 859 - 867 (2008)

Diblock copolymers with one block of poly[((2-dimethylamino)ethyl methacrylate)-co-(glycidyl methacrylate)] P(DMAEMA-c-GMA) and another of poly(pentachlorophenyl acrylate) (PPCPA) (P(DMAEMA-c-GMA)-b-PPCPA) were synthesized via consecutive atom transfer radical polymerization (ATRP). Electrospinnning of P(DMAEMA-c-GMA)-b-PPCPA from a solution in THF and DMF gave rise to microfibers with diameters in the range of 300 nm to 1.3 μ m. Solvent-resistant microfibers were obtained by the subsequent treatment with 1,6-hexanediamine. The quaternary ammonium salts (QASs) were generated viaN-alkylation of tertiary amine groups of the P(DMAEMA-c-GMA) block by the chloro-aromatic compounds of the PPCPA block (or self-quaternization of P(DMAEMA-c-GMA)-b-PPCPA). Combination of the hydrophobic interaction of the PPCPA and the electrostatic interaction of QASs from the self-quaternization of P(DMAEMA-c-GMA)-b-PPCPA gives the resulting microfibers a high antibacterial activity. The antibacterial effect of the crosslinked microfibers was assayed with Escherichia coli and Staphylococcus aureus cultures. 95% E. coli and 97% S. aureus were killed after being contacted with 50 mg P(DMAEMA-c-GMA)-b-PPCPA microfibers in 10 min. The permanence of the antibacterial activity of the self-quaternized P(DMAEMA-c-GMA)-b-PPCPA microfibers was also demonstrated in repeated applications. The Royal Society of Chemistry 2008.

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