Interesting facts
Interesting Facts about 4-Chlorobenzene-1,3-diol
4-Chlorobenzene-1,3-diol, also known as p-chlorophenol, is an intriguing chemical compound with a variety of applications and properties. Here are some notable points of interest:
- Structure and Reactivity: This compound belongs to the family of chlorinated phenols and exhibits a unique substituted aromatic ring. The presence of both hydroxyl (–OH) groups and a chlorine atom makes it an important intermediate in organic synthesis.
- Biological Significance: The compound has been studied for its potential biological activities. It is known to possess antimicrobial properties, making it valuable in the development of disinfectants and preservatives.
- Industrial Uses: 4-Chlorobenzene-1,3-diol is utilized in the production of herbicides, insecticides, and other agrochemicals. Its ability to act as a building block in various chemical reactions enhances its industrial relevance.
- Environmental Impact: As a chlorinated compound, it is essential to understand the environmental implications of its use. Research has been conducted to assess its degradation pathways and potential toxicity to aquatic organisms.
- Historical Context: The synthesis and study of chlorinated phenols date back to the early 20th century. Their relevance in chemical research has garnered attention in fields such as medicinal chemistry and environmental science.
- Health Precautions: Due to its reactivity, appropriate safety measures should be taken when handling this compound. It’s important to research its health effects, particularly in occupational settings.
In conclusion, 4-chlorobenzene-1,3-diol is more than just a simple compound; it showcases how one molecule can have diverse implications across different scientific domains, from industrial applications to environmental concerns.
Synonyms
4-Chlororesorcinol
95-88-5
4-chlorobenzene-1,3-diol
1,3-Benzenediol, 4-chloro-
p-Chlororesorcinol
4-Chlororesorcin
6-Chlororesorcinol
Resorcinol, 4-chloro-
4-Chloro-1,3-dihydroxybenzene
2,4-Dihydroxychlorobenzene
4-Chloro-1,3-benzenediol
C.I. 76510
MFCD00002273
1,3-Dihydroxy-4-chlorobenzene
NSC 1569
EINECS 202-462-0
BRN 2042864
1-Chloro-2,4-dihydroxybenzene
CI 76510
UNII-87045U29QJ
AI3-03873
RODOL CRS
NSC-1569
NSC-6298
COVASTYLE LP-4CLR
87045U29QJ
DTXSID8052643
CI-76510
WLN: QR CQ DG
4-Chlorobenzene-1,3-diol (4-Chlororesorcinol)
4Chlororesorcin
pChlororesorcinol
6Chlororesorcinol
4-chlororesorcine
Resorcinol, 4chloro
4Chloro1,3benzenediol
4Chlorobenzene1,3diol
2,4Dihydroxychlorobenzene
1,3Benzenediol, 4chloro
COLIPA A12
1Chloro2,4dihydroxybenzene
4-Chlororesorcinol, 98%
4Chloro1,3dihydroxybenzene
SCHEMBL33883
4-Chloro-benzene-1,3-diol
DTXCID5031216
NSC1569
NSC6298
4-CHLORORESORCINOL [INCI]
MSK000720
AKOS000121522
CS-W016374
FC34161
HY-W015658
AS-12812
BP-11746
SY026641
1ST000720
NS00002206
EN300-21163
F19551
Q27269773
F0001-2284
Z104493216
[4-[bis[4-(dimethylamino)phenyl]methylene]cyclohexa-2,5-dien-1-ylidene]-dimethyl-ammonium
202-462-0
Solubility of 4-chlorobenzene-1,3-diol (C6H5ClO2)
4-chlorobenzene-1,3-diol exhibits interesting solubility characteristics that are influenced by its molecular structure and functional groups. Here are some key points to consider:
In summary, the solubility of 4-chlorobenzene-1,3-diol in polar solvents is significantly higher due to its polar functional groups and ability to form hydrogen bonds. Understanding these factors can aid in its application in various chemical processes and formulations.