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1-(4-chlorophenyl)non-1-en-3-ol is a chemical compound characterized by its molecular formula C15H21ClO. It features a long-chain unsaturated alcohol structure with a phenyl group connected to the first carbon of the non-1-ene chain. The presence of a chlorophenyl group, which introduces a chlorine atom to the phenyl ring, endows the compound with a chlorinated aromatic structure. This unique molecular architecture suggests potential applications in organic synthesis, pharmaceuticals, and research, with its specific uses contingent upon its reactivity, stability, and compatibility with other compounds.

53710-42-2

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53710-42-2 Usage

Uses

Used in Organic Synthesis:
1-(4-chlorophenyl)non-1-en-3-ol is used as an intermediate in the synthesis of various organic compounds due to its unique chlorinated aromatic structure and long-chain unsaturated alcohol backbone. Its reactivity and stability make it a valuable building block for creating complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(4-chlorophenyl)non-1-en-3-ol is used as a precursor for the development of new drugs. Its specific interactions with other compounds and its unique structure may contribute to the creation of novel therapeutic agents.
Used in Research:
1-(4-chlorophenyl)non-1-en-3-ol is also utilized in research settings to study the effects of chlorinated aromatic structures on chemical reactions and biological activities. This knowledge can be applied to the design of new molecules with specific properties and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 53710-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,1 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53710-42:
(7*5)+(6*3)+(5*7)+(4*1)+(3*0)+(2*4)+(1*2)=102
102 % 10 = 2
So 53710-42-2 is a valid CAS Registry Number.

53710-42-2Downstream Products

53710-42-2Relevant academic research and scientific papers

Nickel-Catalyzed Highly Selective Hydroalkenylation of Alkenyl Boronic Esters to Access Allyl Boron

Zhang, Penglin,Zhang, Min,Ji, Yuqi,Xing, Mimi,Zhao, Qian,Zhang, Chun

, p. 8285 - 8290 (2020/11/12)

Allyl boron derivatives are valuable building blocks in the synthesis of natural products and bioactive molecules. Herein, a practical strategy of nickel-catalyzed highly selective hydroalkenylation of alkenyl boronic esters was developed. Under the mild

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