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Dichloro-phenyl-methyl, also known as 2,4-dichlorophenyl methyl ether, is an organic compound with the chemical formula C7H6Cl2O. It is a colorless to pale yellow liquid that is insoluble in water but soluble in organic solvents. dichloro-phenyl-methyl is primarily used as an intermediate in the synthesis of various agrochemicals, pharmaceuticals, and other chemical products. Due to its reactivity and potential health hazards, it is important to handle dichloro-phenyl-methyl with proper safety measures, including the use of personal protective equipment and proper ventilation.

3170-67-0

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3170-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3170-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3170-67:
(6*3)+(5*1)+(4*7)+(3*0)+(2*6)+(1*7)=70
70 % 10 = 0
So 3170-67-0 is a valid CAS Registry Number.

3170-67-0Downstream Products

3170-67-0Relevant academic research and scientific papers

Fluorescence from samarium(II) iodide and its electron transfer quenching: Dynamics of the reaction of benzyl radicals with Sm(II)

Skene,Scaiano,Cozens

, p. 7918 - 7921 (2007/10/03)

The luminescence from SmI2 in THF can be readily quenched by a variety of electron acceptors. In the case of organohalides, the reaction is quite fast; for example, for dichloromethane the rate constant is 2.7 × 108 M-1 s

Reaction of phenylchlorocarbene and diphenylcarbene with the carbon-chlorine bond: Kinetics and mechanisms

Jones, Michelle B.,Maloney, Vincent M.,Platz, Matthew S.

, p. 2163 - 2169 (2007/10/02)

The reactions of phenylchlorocarbene (PCC) and diphenylcarbene (DPC) with carbon-chlorine bonds were investigated by laser flash photolysis techniques, product studies, and electrochemical methods. The data with both carbenes are consistent with a polar chlorine atom transfer to form radical pairs. The PCC reaction can be thought of as an inner sphere electron transfer from the carbene to the carbon-halogen bond in which there is partial carbon-halogen bond formation in the transition state. The transition state is thought to involve a crossing between closed- and open-shell singlet surfaces. The data obtained in the reaction of DPC with chlorine donors resembles the data obtained with PCC but is more difficult to interpret because the multiplicity of the state reacting with the C-Cl bond is unclear.

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