Interesting facts
Interesting Facts about 1-(Chloromethyl)naphthalene
1-(Chloromethyl)naphthalene is a fascinating compound that belongs to the class of halogenated aromatic hydrocarbons. It is particularly interesting due to its unique chemical structure and various applications. Here are some compelling insights about this compound:
- Chloromethyl Group: The presence of the chloromethyl group in this compound enhances its reactivity, allowing it to participate in a variety of substitution reactions, which is valuable in organic synthesis.
- Precursor in Synthesis: 1-(Chloromethyl)naphthalene serves as a precursor for the synthesis of diverse organic compounds, including pharmaceuticals, dyes, and agrochemicals.
- Uses in Research: This compound is often utilized in scientific research, particularly in the study of reaction mechanisms involving aryl halides and their transformations.
- Environmental Considerations: Like many chlorinated compounds, it is important to handle 1-(chloromethyl)naphthalene with care due to potential environmental and health impacts. Efforts are made to understand its degradation pathways in nature.
- Historical Significance: The study of halogenated compounds has significantly advanced our understanding of aromatic chemistry; hence, 1-(chloromethyl)naphthalene fits into a broader context of chemical evolution.
In summary, 1-(chloromethyl)naphthalene not only plays a crucial role in various synthetic methodologies but also illustrates the intricate interplay of structure and reactivity in organic chemistry. As noted by fundamental research, “Every compound holds a key to understanding larger patterns in chemical behavior." The world of chemical compounds like this one continues to captivate scientists and students alike.
Synonyms
1-(CHLOROMETHYL)NAPHTHALENE
86-52-2
1-Chloromethyl naphthalene
Naphthalene, 1-(chloromethyl)-
1-Chloromethylnaphthalene
1-Naphthylmethyl chloride
1-Menaphthyl chloride
(Chloromethyl)naphthalene
35255-58-4
Naphthalene, 1-chloromethyl-
1-(Chlormethyl)naftalen
alpha-Naphthylmethyl chloride
NSC 8473
alpha-(Chloromethyl)naphthalene
Naphthalene, alpha-chloromethyl-
1-(Chlormethyl)naftalen [Czech]
1-(chloromethyl)naphtalene
EINECS 201-678-2
KD3RZ3R8C4
1-(chloromethyl)-naphthalene
BRN 0636885
.alpha.-(Chloromethyl)naphthalene
NSC-8473
MFCD00004042
1-Chloromethyl-naphthalene
1-(chloromethyl) naphthalene
.alpha.-Naphthylmethyl chloride
DTXSID5058939
4-05-00-01692 (Beilstein Handbook Reference)
Naphthalene, .alpha.-(chloromethyl)-
Naphthalene, (chloromethyl)-
1-Naphthalenylmethyl Chloride; 1-Naphthalylmethyl Chloride; 1-Naphthylmethyl Chloride; NSC 8473; a-(Chloromethyl)naphthalene; a-Naphthylmethyl Chloride
EINECS 252-469-8
1Menaphthyl chloride
Chloromethylnaphthalene
1(Chlormethyl)naftalen
1Naphthylmethyl chloride
1-chloromethylnaphthaline
1-Chloromethyinaphthalene
1Chloromethyl naphthalene
AI3-15963
1-chloromethyl-naphthalen
a-Naphthylmethyl Chloride
alphachloromethylnaphthalene
Naphthalene, 1chloromethyl
naphth-1-ylmethyl chloride
alphaNaphthylmethyl chloride
UNII-KD3RZ3R8C4
alpha-chloromethylnaphthalene
(1-naphthyl)methyl chloride
1-naphthalenylmethyl chloride
alpha(Chloromethyl)naphthalene
alpha-chloromethyl-naphthalene
Naphthalene, 1(chloromethyl)
Naphthalene, alphachloromethyl
SCHEMBL248239
WLN: L66J B1G
(1-naphthalenyl)methyl chloride
DTXCID0048505
NSC8473
1-(Chloromethyl)naphthalene, 90%
AKOS000120764
AC-5784
CS-W017388
FC14789
NSC 405486
LS-13927
NS00039132
EN300-18307
E70399
Q63395890
1-(Chloromethyl)naphthalene, technical, >=97.0% (GC)
F2190-0269
InChI=1/C11H9Cl/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H
201-678-2
Solubility of 1-(Chloromethyl)naphthalene
1-(Chloromethyl)naphthalene, a compound characterized by the presence of a chloro group and a naphthalene moiety, demonstrates distinct solubility properties. Understanding its solubility behavior is essential for its applications in various chemical processes.
Generally, the solubility of 1-(chloromethyl)naphthalene can be summarized as follows:
In summary, while 1-(chloromethyl)naphthalene can find good solubility in nonpolar solvents, it remains considerably insoluble in polar solvents, particularly water. This distinction is crucial for chemists when considering its utility in synthesis and various applications.