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(4-Iodo-phenyl)-[(E)-3-phenyl-prop-2-en-(E)-ylidene]-amine is a complex organic compound characterized by its unique molecular structure. It features a 4-iodophenyl group, which is a phenyl ring with an iodine atom attached at the 4th position. The compound also contains a (E)-3-phenyl-prop-2-en-(E)-ylidene moiety, which is a conjugated system with a double bond between the prop-2-en-1-one and the phenyl ring, both in the E configuration. The amine group is attached to the 4-iodophenyl group, completing the structure. (4-Iodo-phenyl)-[(E)-3-phenyl-prop-2-en-(E)-ylidene]-amine is significant in the field of organic chemistry, particularly for its potential applications in the synthesis of pharmaceuticals and other specialty chemicals due to its reactive functional groups and conjugated system.

3382-77-2

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3382-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3382-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3382-77:
(6*3)+(5*3)+(4*8)+(3*2)+(2*7)+(1*7)=92
92 % 10 = 2
So 3382-77-2 is a valid CAS Registry Number.

3382-77-2Downstream Products

3382-77-2Relevant academic research and scientific papers

Synthesis, Cytotoxicity and Antimicrobial Evaluation of New Coumarin-Tagged β-Lactam Triazole Hybrid

Awolade, Paul,Cele, Nosipho,Dhawan, Sanjeev,Jonnalagadda, Sreekantha B.,Kaur, Mandeep,Kisten, Prishani,Pillay, Ashona-Singh,Saha, SouravTaru,Singh, Parvesh

, (2020)

A series of coumarin-tagged β-lactam triazole hybrids (10a–10o) were synthesized and tested for their cytotoxic activity against MDA-MB-231 (triple negative breast cancer), MCF-7 (estrogen receptor positive breast cancer (ER+)) and A549 (human lung carcinoma) cancer cell lines including one normal cell line, HEK-293 (human embryonic kidney). Two compounds 10b and 10d exhibited substantial cytotoxic effect against MCF-7 cancer cell lines with IC50 values of 53.55 and 58.62 μm, respectively. More importantly, compounds 10b and 10d were non-cytotoxic against HEK-293 cell lines. Structure–activity relationship (SAR) studies suggested that the nitro and chloro group at the C-3 position of phenyl ring are favorable for anticancer activity, particularly against MCF-7 cell lines. Furthermore, antimicrobial evaluation of these compounds revealed modest inhibition of examined pathogenic strains with compounds 10c and 10i being the most promising antimicrobial agents against Pseudomonas aeruginosa and Candida albicans, respectively.

Modular access to vicinally functionalized allylic (thio)morpholinonates and piperidinonates by substrate-controlled annulation of 1,3-azadienes with hexacyclic anhydrides

Braunstein, Hannah,Langevin, Spencer,Khim, Monique,Adamson, Jonathan,Hovenkotter, Katie,Kotlarz, Lindsey,Mansker, Brandon,Beng, Timothy K.

supporting information, p. 8864 - 8872 (2016/10/03)

A modular substrate-controlled hexannulation of inherently promiscuous 1,3-azadienes with hexacyclic anhydrides, which affords versatile vicinally functionalized allylic lactams, in high yields, regio- and stereoselectivities is described.

GREEN SYNTHESIS OF ARYL ALDIMINES USING ETHYL LACTATE

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Page/Page column 5-6, (2011/08/22)

The present invention relates to a method for preparing aryl aldimines. In particular, the present invention relates to methods of preparing aryl aldimines that uses environmentally friendly solvent systems.

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