1,1,1-trichloro-2-(4-hydroxyphenyl)-2-(4-methoxyphenyl)ethane is a synthetic compound that is not commonly known or studied.
There are a couple of reasons why this could be the case:
1. **Unusual/Incorrect Name:** The name itself might be incorrectly formatted or represent a compound that doesn't exist or has a different, more standard name. It's possible that the name was created for a specific research project and isn't part of the general chemical nomenclature.
2. **Lack of Research:** The compound could be a newly synthesized molecule or a derivative of an existing one that hasn't been extensively studied yet. There might not be enough research done to establish its significance or importance.
**To help you find more information, I need some context:**
* **Where did you encounter this name?** Was it in a scientific paper, a textbook, or another source?
* **What is the research context?** What field of study is this compound related to (e.g., pharmaceuticals, materials science, environmental chemistry)?
With more information, I can try to identify the compound and explain its potential relevance.
ID Source | ID |
---|---|
PubMed CID | 183679 |
CHEBI ID | 34026 |
SCHEMBL ID | 15263150 |
MeSH ID | M0479996 |
Synonym |
---|
unii-y8i9cwq645 |
monodemethylmethoxychlor |
phenol, 4-(2,2,2-trichloro-1-(4-methoxyphenyl)ethyl)- |
4-(2,2,2-trichloro-1-(4-methoxyphenyl)ethyl)phenol |
y8i9cwq645 , |
monohydroxymethoxychlor |
1,1,1-trichloro-2-(4-hydroxyphenyl)-2-(4-methoxyphenyl)ethane |
28463-03-8 |
4-[2,2,2-trichloro-1-(4-methoxyphenyl)ethyl]phenol |
mono-hydroxy methoxychlor |
124042-16-6 |
phenol, 4-(2,2,2-trichloro-1-(4-methoxyphenyl)ethyl)-, labeled with carbon-14 |
2-(4-methoxyphenyl)-2-(4-hydroxyphenyl)-1,1,1-trichloroethane |
2-(p-hydroxyphenyl)-2-(p-methoxyphenyl)-1,1,1-trichloroethane |
phenol, p-(p-methoxy-.alpha.-(trichloromethyl)benzyl)- |
demethyl methoxychlor |
CHEBI:34026 |
SCHEMBL15263150 |
DTXSID0022482 |
Q27115759 |
phenol, 4-[2,2,2-trichloro-1-(4-methoxyphenyl)ethyl]- |
Excerpt | Reference | Relevance |
---|---|---|
" Cytochrome P450 enzymes metabolize MXC to mono-OH MXC (1,1,1-trichloro-2-(4-hydroxyphenyl)-2-(4-methoxyphenyl)ethane [mono-OH]) and bis-OH MXC (1,1,1-trichloro-2,2-bis(4-hydroxyphenyl)ethane [HPTE]), two compounds that are proposed to be more toxic than the parent compound, can interact with the estrogen receptor (ER), and are proposed to be responsible for ovarian toxicity." | ( Methoxychlor metabolites may cause ovarian toxicity through estrogen-regulated pathways. Flaws, JA; Gupta, RK; Miller, KP, 2006) | 0.58 |
Class | Description |
---|---|
diarylmethane | Any compound containing two aryl groups connected by a single C atom. |
[compound class information is derived from 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] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.64) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |