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2-(Chroman-4-ylmethyl)phenol is a chemical compound with the molecular formula C15H14O2. It is a derivative of phenol, featuring a chroman-4-ylmethyl group attached to the 2-position of the phenol ring. Chroman is a cyclic structure consisting of a benzene ring fused to a six-membered oxygen-containing ring, similar to a chromone but with a saturated ring. 2-(chroman-4-ylmethyl)phenol is known for its antioxidant properties and is often used in the synthesis of pharmaceuticals and other organic compounds. It is also found in some natural products and has been studied for its potential biological activities, such as anti-inflammatory and anticancer effects. The compound's structure endows it with unique chemical reactivity and stability, making it a valuable intermediate in organic synthesis.

4986-20-3

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4986-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4986-20-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4986-20:
(6*4)+(5*9)+(4*8)+(3*6)+(2*2)+(1*0)=123
123 % 10 = 3
So 4986-20-3 is a valid CAS Registry Number.

4986-20-3Downstream Products

4986-20-3Relevant academic research and scientific papers

Gold-Catalyzed 1,2-Diarylation of Alkenes

Chintawar, Chetan C.,Patil, Nitin T.,Yadav, Amit K.

supporting information, p. 11808 - 11813 (2020/05/18)

Herein, we disclose the gold-catalyzed 1,2-diarylation of alkenes through the interplay of ligand-enabled AuI/AuIII catalysis with the idiosyncratic π-activation mode of gold complexes. Unlike the classical migratory-insertion-based approach to 1,2-diarylation, the present approach not only circumvents the formation of direct Ar?Ar′ coupling and Heck-type side products but more intriguingly demonstrates reactivity and selectivity complementary to those of previously known metal catalysis (Pd, Ni, or Cu). Detailed investigations to underpin the mechanistic scenario revealed oxidative addition of aryl iodides to an AuI complex to be the rate-limiting step owing to the non-innocent nature of the aryl alkene.

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