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Acetic acid, trifluoro-, pentachlorophenyl ester, also known as pentachlorophenyl trifluoroacetate, is a chemical compound with the molecular formula C8Cl5F3O2. It is an ester derivative of trifluoroacetic acid and pentachlorophenol, characterized by the presence of three fluorine atoms and five chlorine atoms in its structure. Acetic acid, trifluoro-, pentachlorophenyl ester is primarily used as a herbicide and a defoliant, effectively controlling the growth of unwanted vegetation. Due to its chemical properties, it is highly stable and persistent in the environment, which has led to concerns regarding its potential impact on ecosystems and human health. As a result, its use has been restricted or banned in several countries.

5672-86-6

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5672-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5672-86-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5672-86:
(6*5)+(5*6)+(4*7)+(3*2)+(2*8)+(1*6)=116
116 % 10 = 6
So 5672-86-6 is a valid CAS Registry Number.

5672-86-6SDS

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) 2,2,2-trifluoroacetate

1.2 Other means of identification

Product number -
Other names Acetic acid,trifluoro-,pentachlorophenyl ester

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:5672-86-6 SDS

5672-86-6Relevant academic research and scientific papers

Active esters of N-substituted piperazine acetic acids, including isotopically enriched versions thereof

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Page/Page column 14-15, (2008/06/13)

In some embodiments, this invention pertains to active esters of N-substituted piperazine acetic acid, including isotopically enriched versions thereof. In some embodiments, this invention pertains to methods for the preparation of active esters of N-subs

Isotopically enriched N-substituted piperazines and methods for the preparation thereof

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Page/Page column 14-15, (2008/06/13)

In some embodiments, this invention pertains to isotopically enriched N-substituted piperazines. In some embodiments, this invention pertains to methods for the preparation of isotopically enriched N-substituted piperazines.

Isotopically enriched N-substituted piperazine acetic acids and methods for the preparation thereof

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Page/Page column 14-15, (2008/06/13)

In some embodiments, this invention pertains to isotopically enriched N-substituted piperazine acetic acids. In some embodiments, this invention pertains to methods for the preparation of isotopically enriched N-substituted piperazine acetic acids.

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