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Mercury, chloro(3-chlorophenyl)-, also known as 2-chloromercuri-3-chlorophenol or chlorophenylmercury, is a chemical compound with the formula C6H4Cl2HgO. It is an organomercury compound, which means it contains a carbon-mercury bond. This particular compound is characterized by the presence of two chlorine atoms and a mercury atom attached to a phenol group. It is a toxic substance and has been used in the past as a fungicide, particularly in seed treatments. Due to its high toxicity and potential for environmental and health hazards, its use has been restricted or banned in many countries. The compound is also known for its potential to bioaccumulate in the environment, posing a risk to wildlife and human health through the food chain.

5955-16-8

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5955-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5955-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5955-16:
(6*5)+(5*9)+(4*5)+(3*5)+(2*1)+(1*6)=118
118 % 10 = 8
So 5955-16-8 is a valid CAS Registry Number.

5955-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-phenylmercury (1+); chloride

1.2 Other means of identification

Product number -
Other names 3-Chlor-phenylquecksilber(1+)

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:5955-16-8 SDS

5955-16-8Downstream Products

5955-16-8Relevant academic research and scientific papers

Substituent effects in aromatic substitution of aryltriethyltin compounds by mercuric halides

Sedaghat-Herati, M. Reza,Sharifi, Taghi

, p. 39 - 44 (2007/10/02)

Second-order rate constants are reported for the reaction of some YC6H4SnEt3 compounds with mercuric halides in tetrahydrofuran, and show that the reaction is one of low selectivity.The substituent effects can be correlated only in terms of Hammett ?-constants, and the data for the meta-methoxy group are anomalous.The results indicate that the rate determining step involves reaction of a ?-complex.Activation parameters are reported, and are in accordance with the suggested mechanism.

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