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(2-iodophenyl)(thiophen-2-yl)methanone is an organic compound characterized by a unique structure that combines a 2-iodophenyl group with a thiophene-2-yl group, both attached to a central methanone (or ketone) moiety. This molecule, with its iodine atom in the ortho position of the phenyl ring and the thiophene ring directly linked to the carbonyl group, exhibits interesting chemical properties. It is a member of the class of compounds known as iodinated ketones and is often used in the synthesis of various pharmaceuticals and organic compounds due to its reactivity and the presence of the halogen atom, which can participate in a range of chemical reactions. The compound's specific structure allows for potential applications in areas such as material science and medicinal chemistry, where its electronic and steric properties can influence the behavior of molecules in complex systems.

6933-33-1

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6933-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6933-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6933-33:
(6*6)+(5*9)+(4*3)+(3*3)+(2*3)+(1*3)=111
111 % 10 = 1
So 6933-33-1 is a valid CAS Registry Number.

6933-33-1Downstream Products

6933-33-1Relevant academic research and scientific papers

Synthesis, characterisation, and reactivity of novel pseudocyclic hypervalent iodine reagents with heteroaryl carbonyl substituents

Qurban, Jihan,Elsherbini, Mohamed,Alharbi, Haifa,Wirth, Thomas

supporting information, p. 7998 - 8000 (2019/07/12)

Two new hypervalent iodine reagents containing furan and thiophene moieties in addition to a carbonyl group in the vicinity of the iodine atom were synthesised and characterised. The X-ray analysis of both compounds revealed a strong intramolecular contact between the carbonyl oxygen and the hypervalent iodine atom with tosylate as a counter ion. The two reagents showed a broad range of synthetic applications and proved to be versatile oxidizing agents.

Cu(I)-Catalyzed Coupling and Cycloisomerization of Diazo Compounds with Terminal Yne-Alkylidenecyclopropanes: Synthesis of Functionalized Cyclopenta[ b]naphthalene Derivatives

Li, Peng-Hua,Yu, Liu-Zhu,Zhang, Xiao-Yu,Shi, Min

, p. 4516 - 4520 (2018/08/09)

A Cu(I)-catalyzed coupling and cycloisomerization of diazo compounds with terminal yne-alkylidenecyclopropanes (ACPs) has been presented. This reaction starts from the formation of an allenic intermediate in the Cu(I)-catalyzed cross-coupling reaction of a diazo compound with terminal alkyne in yne-tethered ACP and then undergoes a domino cycloisomerization of a 6π-electrocyclization and cyclopropane ring-opening rearrangement to give functionalized cyclopenta[b]naphthalene derivatives in moderate to excellent yields under mild conditions.

Palladium-Catalyzed Acylations: One-Pot Synthesis of Indenones

Suchand, Basuli,Satyanarayana, Gedu

supporting information, p. 372 - 381 (2017/04/26)

An efficient, one-pot synthesis of substituted indenones was accomplished starting from simple o-iodoketones and aldehydes. [Pd]-catalyzed direct acylation of o-iodoketones with aldehydes was employed as the key step. Subsequent intramolecular aldol condensation afforded the indenones. Notably, a variety of indenones were achieved. Significantly, the natural product neolignan was accomplished in one pot.

Copper-catalyzed cascade cyclization of 1,5-enynes: Via consecutive trifluoromethylazidation/diazidation and click reaction: Self-assembly of triazole fused isoindolines

Yu, Liu-Zhu,Wei, Yin,Shi, Min

supporting information, p. 13163 - 13166 (2016/11/09)

Copper-catalyzed cascade cyclization of 1,5-enynes with two types of hypervalent reagents was developed via consecutive trifluoromethylazidation/diazidation and intramolecular click reaction (CUAAC), providing one-pot self-assembly of triazole fused isoindolines bearing a trifluoromethyl or an azide moiety. Moreover, the construction of a trifluoromethylcyclopropyl unit, which has been considered as a metabolically stable replacement for a tert-butyl moiety and was difficult to access, was also achieved under trifluoromethylazidation conditions. All these reactions exhibited excellent chemoselectivity, good to excellent yields and broad functional group tolerance.

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