1-(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl-)-1-pentanone

Description

The provided name, 1-(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl-)-1-pentanone, describes a specific organic molecule. It's a bit of a mouthful, so let's break it down:

* **1-pentanone:** This is the base molecule. It's a five-carbon chain with a ketone group (C=O) on the first carbon.
* **(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl-)**: This describes a substituent group attached to the first carbon of pentanone. Let's break this down further:
* **phenyl-**: This indicates a benzene ring (six-membered carbon ring with alternating double bonds).
* **(3,5-dichloro-2,6-dihydroxy-4-methoxy-)**: These are the substituents on the benzene ring.
* **3,5-dichloro**: Chlorine atoms are attached to the 3rd and 5th positions of the benzene ring.
* **2,6-dihydroxy**: Hydroxyl groups (OH) are attached to the 2nd and 6th positions of the benzene ring.
* **4-methoxy**: A methoxy group (OCH3) is attached to the 4th position of the benzene ring.

**Why is this molecule important for research?**

Unfortunately, the name alone doesn't give much information about its potential importance. To understand its significance, we need to know:

* **What are its properties?** Does it have unique physical or chemical properties? Is it reactive? Is it stable?
* **What are its potential uses?** Is it a potential drug candidate? Does it have biological activity? Does it exhibit any catalytic properties?
* **What research is being done with it?** This molecule may be part of ongoing studies in medicine, materials science, or other fields.

**To find out why this specific molecule is important, you would need to:**

1. **Look for it in scientific databases:** Search databases like PubChem, SciFinder, or Google Scholar using the full chemical name or structure. These databases often contain information about known compounds, including their properties, synthesis methods, and relevant publications.
2. **Check for patents:** Patents are often a good indicator of the potential commercial value of a molecule.
3. **Read research publications:** Search for publications that mention this molecule in their titles, keywords, or abstract.

Without further context, it's impossible to definitively say why this specific molecule is important for research. However, the combination of a ketone group with a substituted benzene ring can lead to a variety of interesting properties, making it a potential candidate for exploration in different research areas.

1-(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl-)-1-pentanone: structure given in first source; endogenous differention-inducing factor; induces stalk-cell differentiation in the cellular slime mold Dictyostelium discoideum [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1-(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl)pentan-1-one : A differentiation-inducing factor that is pentaphenone bearing two chloro substituents at positions 3 and 5, two hydroxy substituents at positions 2 and 6 as well as a single methoxy substituent at position 4. A secreted, chlorinated molecule that controls cell fate during development of Dictyostelium cells. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]