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2,6-dichlorophenacyl chloride is a chemical compound with the formula C8H5Cl3O, characterized by the presence of two chlorine atoms at the 2 and 6 positions on the phenyl ring. It is a derivative of phenacyl chloride and is known for its colorless to pale yellow liquid appearance, strong pungent odor, and corrosive and toxic properties. 2,6-dichlorophenacyl chloride is widely utilized in organic synthesis for the introduction of the 2,6-dichlorophenyl group into other molecules and serves as an intermediate in the production of pharmaceuticals and agrochemicals.

81547-71-9

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81547-71-9 Usage

Uses

Used in Organic Synthesis:
2,6-dichlorophenacyl chloride is used as a reagent for the introduction of the 2,6-dichlorophenyl group into other molecules, facilitating the synthesis of various organic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,6-dichlorophenacyl chloride is used as an intermediate in the production of drugs, contributing to the development of new medications with potential therapeutic benefits.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 2,6-dichlorophenacyl chloride is employed as an intermediate for the synthesis of various agrochemicals, including pesticides and herbicides, to enhance crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 81547-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,4 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81547-71:
(7*8)+(6*1)+(5*5)+(4*4)+(3*7)+(2*7)+(1*1)=139
139 % 10 = 9
So 81547-71-9 is a valid CAS Registry Number.

81547-71-9Relevant academic research and scientific papers

REACTIONS OF 2,4- AND 2,6-DICHLOROPHENACYLIDENE HALIDES WITH TRIALKYLPHOSPHITES IN PROTIC SOLVENTS. DIRECT EVIDENCE FOR THE "ENOLATE ANION" PATHWAY

Mlotkowska, Barbara,Majewski, Piotr,Koziara, Anna,Zwierzak, Andrzej,Sledzinski, Bohdan

, p. 631 - 642 (2007/10/02)

The reactions of 2,6-dichlorophenacyl and 2,6-dichlorophenacylidene chlorides and bromides with trimethyl and triethyl phosphites have been investigated.The reactivity of 2,6-dichlorophenacylidene chloride and bromide towards trialkyl phosphites was compared with that of 2,4-dichlorophenacylidene chloride and bromide.The influence of methanol, acting as a model protic solvent, on the above mentioned processes has also benn investigated.The mechanism of Perkow reaction of sterically hindered α-haloketones with bulky substituents around the carbonyl center is discussed.

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