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(3-(4-chlorophenyl)prop-2-yne-1,1-diyl)dibenzene is a chemical compound characterized by a molecular formula of C22H16Cl2. It is a derivative of propyne and dibenzene, featuring a 4-chlorophenyl group attached to the propyne unit. This unique structure and composition endow it with potential applications in various fields.

1246658-59-2

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1246658-59-2 Usage

Uses

Used in Organic Synthesis:
(3-(4-chlorophenyl)prop-2-yne-1,1-diyl)dibenzene is utilized as a key intermediate in organic synthesis for the creation of complex organic molecules. Its distinctive structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-(4-chlorophenyl)prop-2-yne-1,1-diyl)dibenzene is employed as a starting material or a building block for the development of new drugs. Its unique molecular structure can be leveraged to design and synthesize novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Chemical Research:
(3-(4-chlorophenyl)prop-2-yne-1,1-diyl)dibenzene also serves as a subject of interest in chemical research. Scientists and researchers explore its properties, reactivity, and potential interactions with other molecules to gain insights into new chemical reactions and mechanisms, which can lead to the discovery of innovative applications and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 1246658-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,6,5 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1246658-59:
(9*1)+(8*2)+(7*4)+(6*6)+(5*6)+(4*5)+(3*8)+(2*5)+(1*9)=182
182 % 10 = 2
So 1246658-59-2 is a valid CAS Registry Number.

1246658-59-2Downstream Products

1246658-59-2Relevant academic research and scientific papers

Site-Selective Csp3-Csp/Csp3-Csp2Cross-Coupling Reactions Using Frustrated Lewis Pairs

Dasgupta, Ayan,Stefkova, Katarina,Babaahmadi, Rasool,Yates, Brian F.,Buurma, Niklaas J.,Ariafard, Alireza,Richards, Emma,Melen, Rebecca L.

, p. 4451 - 4464 (2021/04/07)

The donor-acceptor ability of frustrated Lewis pairs (FLPs) has led to widespread applications in organic synthesis. Single electron transfer from a donor Lewis base to an acceptor Lewis acid can generate a frustrated radical pair (FRP) depending on the s

Cu(OTf)2-catalyzed arylmethylation of terminal alkynes with benzylic alcohols under ligand-, base-, and additive-free reaction conditions

Ren, Kai,Li, Pinhua,Wang, Lei,Zhang, Xiuli

supporting information; experimental part, p. 2753 - 2759 (2011/04/27)

An effective, convenient, and mild coupling reaction of benzylic alcohols with terminal alkynes has been developed. As an effective Lewis acid, Cu(OTf)2-catalyzed arylmethylation of terminal alkynes with benzylic alcohols generated the correspo

Pd-catalyzed three-component coupling of N-Tosylhydrazone, terminal alkyne, and Aryl halide

Zhou, Lei,Ye, Fei,Zhang, Yan,Wang, Jianbo

experimental part, p. 13590 - 13591 (2010/12/29)

A Pd-catalyzed three-component reaction of N-tosylhydrazone, terminal alkyne, and aryl halide follows a mechanism involving a sequence of Pd carbene migratory insertion-transmetalation-reductive elimination, leading to the formation of one sp2-sp3 C-C bond and one sp-sp 3 C-C bond.

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