Outrageously Funny Search Suggestion Engine :: 1516

👉 Common directory name

C:/1516/

👉 This substance was discovered in 1972 and is known as 1516N-PFP. It's a compound found primarily in nature, commonly occurring in marine sediments. The chemical structure and specific properties make it an important biopharmaceutical agent.

1516. N-(2,5-Dichlorophenyl)-3-(3,4-difluorophenyl)prop-2-enamide; 821004-81-3

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Okay, so I need to define this word that's given as '1516. N (2,5-Dichlorophenyl) 3-(3,4-difluorophenyl)prop-2-enamide; 821004 81 3'. Then come up with an example sentence that's edgy or unsettling. Let me start by breaking down each part of this term. First, the name looks like a chemical compound, probably from organic chemistry. The structure mentions N (which stands for nitrogen), attached to different phenyl groups: one is 2,5-dichlorophenyl and the other is 3,4-difluorophenyl. Then there's prop-2-enamide, which I think is a three-carbon chain with an amide group on the second carbon. Wait, let me parse that again. Prop-2-enamide would be a propanamide where the amide is attached to the second carbon of a propene chain (since prop-2-en means there's a double bond between carbons 1 and 2). So maybe it's something like CH₂=CH-CONH₂? But then how do the substituents fit in? The numbers in parentheses might indicate the positions on the phenyl rings. For example, (2,5-Dichlorophenyl) means the chlorine atoms are attached to carbons 2 and 5 of the benzene ring. Similarly, (3,4-difluorophenyl) would have fluorine atoms at positions 3 and 4. So combining these two phenyl groups with a nitrogen atom in between... Wait, no—the structure is N connected to both phenyl rings via the prop-2-enamide chain. Alternatively, maybe it's an amide where the nitrogen is linked to both chlorophenyl and fluoro-substituted phenyl groups. That would make it a substituted propanamide. Let me visualize this: the central nitrogen is bonded to two aromatic rings (the dichloro and difluorophenyl) via the prop-2-enamide chain. So maybe it's something like: Cl F \ / C6H4-C-C-NHC6H4F2 But with chlorines on the first phenyl at positions 2 and 5, fluorines on the second at 3 and 4. Wait, benzene rings have positions numbered from 1 to 6. So for 2,5-dichlorobenzene, that's substituents at carbons 2 and 5. Similarly, 3,4-difluorophenyl would be fluorines at positions 3 and 4. Putting this together, the prop-2-enamide chain connects these two phenyl groups through the nitrogen. So the structure is: Cl F \ / Ph-C=C-NH-Ar Wait, maybe not exactly. Let me think again. Prop-2-enamide would be CH₂=CH-CONH₂. But with substituents on both ends? No, wait: propanamide is NH₂-CO-CH₂CH₃ or something else? Wait, amide typically has the structure R-C(=O)-NH-R'. So in this case, maybe it's a substituted amide where one side is 2,5-dichlorophenyl and the other is 3,4-difluorophenyl. So the structure would be: Cl F \ / Ph-C-NH-C6H3(F)2Cl Wait, no, maybe it's more like each phenyl group is attached to the prop-2-enamide chain. Let's break it down step by step. The name: 'N (2,5-Dichlorophenyl) 3-(3,4-difluorophenyl)prop 2 enamide'. The 'prop 2 enamde' probably means propanamide where the amide group is attached to carbon 2 of a propenamide chain. Wait, maybe it's better written as N-(2,5-Dichlorophenyl)-3-(3,4-difluorophenyl)propanamide. So the structure would be: Cl F \ / Ph-C-N-CO-Ph' Where the first phenyl (2,5-dichloro) is attached to carbon adjacent to the amide nitrogen, and the second phenyl (3,4-di-fluoro) is also attached to that same nitrogen. Wait, but in an amide group, it's R-C(=O)-NH-R'. So here, both R groups are different: one is 2,5-dichlorophenyl and the other is 3,4-difluorophenyl. So putting it all together, the molecule would have a propanamide backbone where each end (the carbonyl side) has an amide linkage to either phenyl ring. Wait, no—amides are R-CONH-R'. So in this case, maybe it's N-(2,5-dichlorophenyl)-3-(3,4-difluorophenyl)propanamide would be CH₃-CH₂-NH-C(=O)-Ph-Cl and Ph-F? Hmm, not sure. Maybe the propanamide is structured such that each carbon in the three-carbon chain has substituents. Wait, perhaps it's better to draw it out mentally: The amide group is -CONH-. So the structure would be: Cl F \ / C6H3-Cl NOO- \ Ph-F? Wait, this isn't making much sense. Let me check standard nomenclature rules. In organic chemistry, when you have a name like N-substituted-N'-substituted amide, the structure would be R-CONHR' where both R and R' are substituents on the nitrogen of the amide group. So in this case, it's N-(2,5-dichlorophenyl) - CO - NH - (3,4-difluorophenyl). Wait, but that seems like only one substitution? Or maybe each phenyl is attached to the same nitrogen. Wait, perhaps there's a typo in the original name. The user wrote 'prop 2 enamde' which might be "propanamide", and then substituents on both ends of the amide group. Alternatively, could it be that prop-2-enamide has two double bonds? Wait, propenenitrile would be CH₂=CH-CN, but here it's an amide: maybe NC(O)CH=CH2 or something else. Alternatively, "prop 2 enamde" might refer to a three-carbon chain with the amide group on carbon 2. So propanamide is NH₂-CO-OEt or similar, but if it's prop-2-enamide, that would be like CH₂=C(NH₂)COOH? Not sure. Alternatively, maybe "prop-2-enamide" refers to a structure where there's an amide group attached to a propenyl chain. For example, (E)-CH=CHCONH₂ or something similar. But the substituents here are phenyl groups. This is getting