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C15H14ClN is an organic compound with the molecular formula indicating it contains 15 carbon atoms, 14 hydrogen atoms, 1 chlorine atom, and 1 nitrogen atom. C15H14ClN likely belongs to a class of chemicals known as chlorinated aromatic amines, which are derivatives of aromatic amines where one or more hydrogen atoms are replaced by chlorine. These types of compounds can have various applications, such as in pharmaceuticals, agrochemicals, or as intermediates in chemical synthesis. The presence of chlorine and nitrogen in the molecule suggests that it may have unique chemical properties, such as increased lipophilicity due to the chlorine atom, which can affect its solubility and reactivity. The specific properties and uses of C15H14ClN would depend on its exact structure, including the positions of the chlorine and nitrogen atoms on the aromatic ring and any additional functional groups present.

3583-52-6

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3583-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3583-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3583-52:
(6*3)+(5*5)+(4*8)+(3*3)+(2*5)+(1*2)=96
96 % 10 = 6
So 3583-52-6 is a valid CAS Registry Number.

3583-52-6Upstream product

3583-52-6Relevant academic research and scientific papers

Branch-selective synthesis of oxindole and indene scaffolds: Transition metal-controlled intramolecular aryl amidation leading to C3 reverse-prenylated oxindoles

Ignatenko, Vasily A.,Deligonul, Nihal,Viswanathan, Rajesh

supporting information; experimental part, p. 3594 - 3597 (2010/11/04)

In an effort to access biologically important scaffolds, a concise branch-selective synthesis of C3 tertiary oxindoles by Cu(I)-catalyzed aryl amidation and 2,2-dimethyl indene by Pd(0)-catalyzed Heck cyclization has been accomplished from acyclic reverse-prenylated intermediates. Oxindole C3-enolate generation using NaH followed by alkylation in the presence of appropriate electrophiles provides a novel route to quaternary C3 reverse-prenylated oxindoles.

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