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1-[4-(2-Chloroethoxy)-3-methoxyphenyl]ethanone is a complex organic chemical compound with the molecular formula C11H13ClO3. It is a derivative of acetophenone, featuring a chloroethoxy group at the para position and a methoxy group at the meta position on the phenyl ring. 1-[4-(2-Chloroethoxy)-3-methoxyphenyl]ethanone is characterized by its unique structure, which includes a carbonyl group (C=O) attached to the phenyl ring, and a chloroethoxy side chain. It is a colorless to pale yellow liquid with a specific molecular weight of 224.67 g/mol. Due to its chemical structure, it may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. However, it is important to note that the compound's specific uses, safety, and environmental impact should be thoroughly evaluated, as it contains a halogenated ether group, which can be of concern in terms of toxicity and environmental persistence.

3430-03-3

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3430-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3430-03-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3430-03:
(6*3)+(5*4)+(4*3)+(3*0)+(2*0)+(1*3)=53
53 % 10 = 3
So 3430-03-3 is a valid CAS Registry Number.

3430-03-3Relevant academic research and scientific papers

Synthesis of N-aryloxyalkylanabasine derivatives

Slyn'Ko,Tatarova,Shakirov,Shul'Ts

, p. 294 - 301 (2013/07/26)

N-Aryloxyalkylanabasine derivatives were prepared via the reaction of anabasine hydrochloride with various aryloxyhaloalkanes in the presence of potash in DMF. The reaction occurred with retention of the chiral center C-(2) of the piperidine group. Side products of bis(aryloxy)ethanes were characterized.

Arylalkylheterocyclic amines,N-substituted by aryloxyalkyl group in a method for allergy treatment

-

, (2008/06/13)

A method of inhibiting Type 1 allergic responses in a living animal body with substituted heterocyclic amines is disclosed wherein the active agents are expressed generally by the formula which includes certain known and certain known compounds: STR1 wherein P is zero, one or two; m is one to six inclusive; A is selected from hydrogen, hydroxy or cyano; d is zero or one; Q is --CH--, CH2 -- or STR2 n is zero or one and when Q is --CH-- and n is one, a double bond is formed with one of the adjacent carbons but not both at the same time, and when n and d are zero at the same time, a double bond is formed between the α carbon and a carbon of the central heterocyclic amine ring; Ar, D and R are selected from phenyl, substituted phenyl, pyridinyl, thienyl, furanyl or naphthyl and in addition, R may have the values benzyl, substituted benzyl, cycloalkyl or loweralkyl and D may additionally have the values: 2H-1-benzopyran-2-one,4-oxo-4H-1-benzopyran-2-carboxylic acid loweralkyl ester, 2,3-dihydro-4H-1-benzopyran-4-one, 1,4-benzodioxanloweralkyl-2-yl or 1,1'-biphenyl-4-yl and the pharmaceutically acceptable salts thereof.

Synthesis and Antiallergy Activity of 4-(Diarylhydroxymethyl)-1-piperidines and Structurally Related Compounds

Walsh, David A.,Franzyshen, Stephen K.,Yanni, John M.

, p. 105 - 118 (2007/10/02)

A series of 4-(diarylhydroxymethyl)-1-piperidines was synthesized and evaluated for antiallergy activity.Several analogues had potent activity in the passive foot anaphylaxis (PFA) assay, an IgE-mediated model useful in the detection of compounds possessing antiallergic activity.In particular 1--1-piperidinyl>propoxy>-3-methoxyphenyl>ethanone (1, AHR-5333) was more potent than oxatomide and terfenadine in this assay.

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