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2-(2,6-dichlorophenoxy)-6-methylpyridine is a chemical compound with the molecular formula C12H9Cl2NO. It is a derivative of pyridine, featuring a 2,6-dichlorophenoxy group attached to the 2-position and a methyl group at the 6-position. 2-(2,6-dichlorophenoxy)-6-methylpyridine is known for its potential use as an intermediate in the synthesis of various agrochemicals and pharmaceuticals, particularly those with insecticidal and herbicidal properties. Its structure provides a basis for understanding its reactivity and potential applications in chemical research and development.

28369-98-4

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28369-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28369-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,6 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28369-98:
(7*2)+(6*8)+(5*3)+(4*6)+(3*9)+(2*9)+(1*8)=154
154 % 10 = 4
So 28369-98-4 is a valid CAS Registry Number.

28369-98-4Downstream Products

28369-98-4Relevant academic research and scientific papers

Synthesis method and application of 2-(2,6-dichlorophenoxy) pyridine compound

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Paragraph 0255-0265, (2017/08/30)

The invention relates to a synthesis method and application of a 2-(2,6-dichlorophenoxy) pyridine compound. In an organic solvent, 2-phenoxy pyridine and N-chlorosuccinimide are taken as reaction raw materials, and under the joint promotion effect of a tr

Regioselective C-H chlorination: Towards the sequential difunctionalization of phenol derivatives and late-stage chlorination of bioactive compounds

Gao, Chao,Li, Hongchen,Liu, Miaochang,Ding, Jinchang,Huang, Xiaobo,Wu, Huayue,Gao, Wenxia,Wu, Ge

, p. 46636 - 46643 (2017/10/16)

We have developed a protocol for the auxillary directed C-H chlorination of phenol derivatives using catalytic amounts of palladium acetate that is amenable to the late-stage chlorination of diflufenican and estrone. The 2-pyridine group allows for a highly efficient palladium-catalyzed chlorination and sequential ortho C-H functionalization reaction of phenol derivatives to produce a variety of symmetrical and unsymmetrical 2,4,6-trisubstituted phenols.

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