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Zinc, chloro(2,6-dimethylphenyl)is a chemical compound that features a 2,6-dimethylphenyl group attached to zinc and chlorine atoms. It is recognized for its ability to inhibit the growth of various microorganisms, making it a valuable ingredient in antifungal and antimicrobial products. Zinc, chloro(2,6-dimethylphenyl)also plays a significant role in the synthesis of organic compounds and as a catalyst in certain chemical reactions, contributing to its diverse applications in the fields of chemistry and industry.

125102-18-3

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125102-18-3 Usage

Uses

Used in Pesticide Production:
Zinc, chloro(2,6-dimethylphenyl)is used as an active ingredient in the production of pesticides, particularly for controlling and preventing the growth of harmful microorganisms in agricultural settings. Its effectiveness in inhibiting microbial growth helps protect crops from diseases and pests, thereby ensuring higher yields and better quality produce.
Used in Fungicide Production:
In the agricultural industry, Zinc, chloro(2,6-dimethylphenyl)- is utilized as a key component in the formulation of fungicides. Zinc, chloro(2,6-dimethylphenyl)helps combat fungal infections in crops, which can lead to significant losses in yield and quality. Its antifungal properties make it a reliable choice for farmers seeking to protect their plants from various fungal diseases.
Used in Herbicide Production:
Zinc, chloro(2,6-dimethylphenyl)is also employed in the development of herbicides, which are essential for controlling and eliminating unwanted weeds in agricultural fields. Its ability to inhibit the growth of a wide range of plant species makes it a valuable tool in maintaining healthy and productive croplands.
Used in Organic Synthesis:
Zinc, chloro(2,6-dimethylphenyl)is used as a reagent in the synthesis of various organic compounds. Its unique properties allow it to participate in a range of chemical reactions, contributing to the creation of new and useful chemical entities.
Used as a Catalyst in Chemical Reactions:
Zinc, chloro(2,6-dimethylphenyl)is utilized as a catalyst in certain chemical processes, where it helps to increase the rate of reaction and improve the overall efficiency of the process. Its catalytic properties make it a valuable asset in the field of chemistry, particularly in industrial applications where speed and efficiency are crucial.

Check Digit Verification of cas no

The CAS Registry Mumber 125102-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125102-18:
(8*1)+(7*2)+(6*5)+(5*1)+(4*0)+(3*2)+(2*1)+(1*8)=73
73 % 10 = 3
So 125102-18-3 is a valid CAS Registry Number.

125102-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name chlorozinc(1+),1,3-dimethylbenzene-2-ide

1.2 Other means of identification

Product number -
Other names Zinc,chloro(2,6-dimethylphenyl)

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:125102-18-3 SDS

125102-18-3Relevant academic research and scientific papers

Remote Stereoinduction in the Organocuprate-Mediated Allylic Alkylation of Allylic gem-Dichlorides: Highly Diastereoselective Synthesis of (Z)-Chloroalkene Dipeptide Isosteres

Kobayakawa, Takuya,Narumi, Tetsuo,Tamamura, Hirokazu

, p. 2302 - 2305 (2015)

Highly diastereoselective synthesis of (Z)-chloroalkene dipeptide isosteres has been achieved by 1,4-asymmetric induction in the organocuprate-mediated allylic alkylation adjacent to the chiral center of allylic gem-dichlorides. The reaction proceeds with

A CONVENIENT SYNTHESIS OF 5-ARYLTROPONES

Keenan, Richard M.,Kruse, Lawrence I.

, p. 793 - 798 (2007/10/02)

2-methoxy-5-oxy>tropone was coupled to a variety of arylzinc chlorides in the presence of a palladium catalyst to furnish 5-aryltropones in good to excelent yields.

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