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1-(2-chloro-4-methoxyphenyl)piperidine is a chemical compound with the molecular formula C12H16ClNO. It is a white to off-white crystalline solid and is classified as a piperidine derivative, which is a type of heterocyclic amine. 1-(2-chloro-4-methoxyphenyl)piperidine features a piperidine ring with a 2-chloro-4-methoxyphenyl group attached to the nitrogen atom. The presence of the chloro and methoxy substituents on the phenyl ring imparts unique chemical properties to the molecule, making it a potential candidate for various applications in the pharmaceutical and chemical industries. Due to its complex structure, it is typically synthesized through multi-step reactions and is used as an intermediate in the preparation of more complex organic compounds.

4580-84-1

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4580-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4580-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4580-84:
(6*4)+(5*5)+(4*8)+(3*0)+(2*8)+(1*4)=101
101 % 10 = 1
So 4580-84-1 is a valid CAS Registry Number.

4580-84-1Downstream Products

4580-84-1Relevant academic research and scientific papers

Metal-free late-stage C(sp2)-H functionalization of: N -aryl amines with various sodium salts

Mudithanapelli, Chandrashekar,Kim, Mi-Hyun

, p. 450 - 464 (2020)

Metal-free consecutive C(sp2)-X (X = Cl, Br, S, N) bond formations of N-aryl amines (cyclic, fused, carbamate, and aminium radicals) were achieved under mild conditions using [bis(trifluoroacetoxy)iodo]benzene (PIFA) and simple nonharmful sodium salts. This direct and selective C(sp2)-H functionalization showed excellent functional group compatibility, cost effectiveness, and late-stage applicability for the synthesis of biologically active natural products. Two mechanisms were proposed to explain the ortho- or para-preference, as well as the accelerating effect of CH3NO2

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