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(3-bromo-2-methoxy-5-methylphenyl)(phenyl)methanone is a complex organic compound with the molecular formula C15H13BrO2. It is a derivative of benzophenone, featuring a bromine atom at the 3-position, a methoxy group at the 2-position, and a methyl group at the 5-position on the phenyl ring. (3-bromo-2-methoxy-5-methylphenyl)(phenyl)methanone is characterized by its unique structure, which contributes to its chemical properties and potential applications. It is often used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatility in forming different chemical bonds and its ability to influence the reactivity and stability of the molecules in which it is incorporated.

6723-10-0

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6723-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6723-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6723-10:
(6*6)+(5*7)+(4*2)+(3*3)+(2*1)+(1*0)=90
90 % 10 = 0
So 6723-10-0 is a valid CAS Registry Number.

6723-10-0Upstream product

6723-10-0Relevant academic research and scientific papers

Redox-Neutral Coupling between Two C(sp3)?H Bonds Enabled by 1,4-Palladium Shift for the Synthesis of Fused Heterocycles

Rocaboy, Ronan,Anastasiou, Ioannis,Baudoin, Olivier

supporting information, p. 14625 - 14628 (2019/09/16)

The intramolecular coupling of two C(sp3)?H bonds to forge a C(sp3)?C(sp3) bond is enabled by 1,4-Pd shift from a trisubstituted aryl bromide. Contrary to most C(sp3)?C(sp3) cross-dehydrogenative couplings, this reaction operates under redox-neutral conditions, with the C?Br bond acting as an internal oxidant. Furthermore, it allows the coupling between two moderately acidic primary or secondary C?H bonds, which are adjacent to an oxygen or nitrogen atom on one side, and benzylic or adjacent to a carbonyl group on the other side. A variety of valuable fused heterocycles were obtained from easily accessible ortho-bromophenol and aniline precursors. The second C?H bond cleavage was successfully replaced with carbonyl insertion to generate other types of C(sp3)-C(sp3) bonds.

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