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4-iodo-1-iodoethynylbenzene is an organic compound characterized by its unique structure, which features a benzene ring with two iodine atoms attached to different positions. Specifically, one iodine atom is located at the 4-position (para to the ethynyl group), while the other is attached to the terminal carbon of the ethynyl group (1-position). This molecule is of interest in organic synthesis due to its potential applications in the formation of various functional groups and its reactivity towards different chemical transformations. The presence of two iodine atoms enhances its reactivity, making it a valuable intermediate in the synthesis of more complex molecules, particularly in pharmaceuticals and materials science.

934-96-3

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934-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 934-96-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 934-96:
(5*9)+(4*3)+(3*4)+(2*9)+(1*6)=93
93 % 10 = 3
So 934-96-3 is a valid CAS Registry Number.

934-96-3Relevant academic research and scientific papers

Regioselective Synthesis of Polyheterohalogenated Naphthalenes via the Benzannulation of Haloalkynes

Lehnherr, Dan,Alzola, Joaquin M.,Lobkovsky, Emil B.,Dichtel, William R.

supporting information, p. 18122 - 18127 (2015/12/24)

Independent control of halide substitution at six of the seven naphthalene positions of 2-arylnaphthalenes is achieved through the regioselective benzannulation of chloro-, bromo-, and iodoalkynes. The modularity of this approach is demonstrated through the preparation of 44 polyheterohalogenated naphthalene products, most of which are difficult to access through known naphthalene syntheses. The outstanding regioselectivity of the reaction is both predictable and proven unambiguously by single-crystal X-ray diffraction for many examples. This synthetic method enables the rapid preparation of complex aromatic systems poised for further derivatization using established cross-coupling methods. The power and versatility of this approach makes substituted naphthalenes highly attractive building blocks for new organic materials and diversity-oriented synthesis.

Supramolecular hierarchy among halogen-bond donors

Aakeroey, Christer B.,Baldrighi, Michele,Desper, John,Metrangolo, Pierangelo,Resnati, Giuseppe

, p. 16240 - 16247 (2013/12/04)

Through a combination of structural chemistry, vibrational spectroscopy, and theory, we have systematically examined the relative structure-directing importance of a series of ditopic halogen-bond (XB) donors. The molecular electrostatic potential surfaces of six XB donors were evaluated, which allowed for a charge-based ranking. Each molecule was then co-crystallized with 21 XB acceptors and the results have made it possible to map out the supramolecular landscape describing the competition between I/Br-ethynyl donors, perfluorinated I/Br donors, and I/Br-phenyl based donors. The results offer practical guidelines for synthetic crystal engineering driven by robust and directional halogen bonds. Copyright

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