Interesting facts
Interesting Facts about 1-Bromonaphthalen-2-ol
1-Bromonaphthalen-2-ol, a fascinating compound in the field of organic chemistry, is rich in molecular intricacies and applications. Here are some intriguing aspects of this compound:
- Structure and Versatility: The compound features a naphthalene backbone, which is a fused ring system, providing unique physical and chemical properties. This makes it an excellent candidate for various chemical reactions.
- Functional Groups: The presence of a hydroxyl (-OH) group contributes to its reactivity, playing a crucial role in hydrogen bonding and enhancing solubility in polar solvents.
- Applications: 1-Bromonaphthalen-2-ol is utilized in organic synthesis as an important intermediate. It can serve as a starting material for the preparation of dyes, pharmaceuticals, and agrochemicals.
- Chemical Reactions: It readily undergoes nucleophilic substitution reactions, making it a valuable tool for chemists aiming to create more complex molecules.
- Historical Significance: The bromination of naphthalene, leading to compounds such as this one, has been a fundamental reaction in synthetic organic chemistry since its early discovery, shedding light on the evolution of chemical techniques.
As a fascinating blend of structure and functionality, 1-bromonaphthalen-2-ol stands out as a compound that showcases the beauty of organic synthesis. Whether it’s for educational purposes or industrial applications, understanding its properties can unlock numerous pathways in chemical research and development.
Synonyms
1-Bromo-2-naphthol
573-97-7
2-Naphthalenol, 1-bromo-
1-Bromo-2-naphthalenol
Wormin
Disthemin
1-Brom-2-naphthol
1-Bromo-2-hydroxynaphthalene
2-NAPHTHOL, 1-BROMO-
1-Brom-2-naphthol [German]
1-Bromo-.beta.-naphthol
EINECS 209-363-1
VKE7L55PP9
NSC 60275
BRN 2044001
.alpha.-Bromo-.beta.-naphthol
NSC-60275
DTXSID20205919
4-06-00-04301 (Beilstein Handbook Reference)
1Brom2naphthol
1Bromo2naphthalenol
2Naphthol, 1bromo
1-Bromo-beta-naphthol
2Naphthalenol, 1bromo
alpha-Bromo-beta-naphthol
2Naphthalenol, 1bromo (9CI)
DTXCID00128410
2-Naphthalenol, 1-bromo-(9CI)
209-363-1
1-bromonaphthalen-2-ol
MFCD00003869
MLS000069595
NSC60275
SMR000059032
UNII-VKE7L55PP9
1-Bromo-2-naphthalenol , 2-Naphthol, 1-bromo- (7CI, 8CI), 1-Bromo-2-hydroxynaphthalene, 1-Bromo-2-naphthol
1-bromonaphth-2-ol
1-Bromo-naphtalen-2-ol
1-bromo-naphthalen-2-ol
1-bromanylnaphthalen-2-ol
SCHEMBL49630
cid_11316
1-Bromo-2-naphthol, 97%
CHEMBL1414294
BDBM51324
HMS2231M12
HMS3369D15
STR06183
STK068802
AKOS000121002
CS-W007565
NCGC00247018-01
AC-22890
SY020306
TS-00532
DB-019066
B0620
NS00033711
EN300-17300
A23764
AE-641/30106059
Q27291869
Z56913130
InChI=1/C10H7BrO/c11-10-8-4-2-1-3-7(8)5-6-9(10)12/h1-6,12
Solubility of 1-bromonaphthalen-2-ol
1-bromonaphthalen-2-ol, with its unique structure, exhibits intriguing solubility characteristics that are essential to its chemical behavior. Understanding its solubility in various solvents can enhance our insight into its potential applications and interactions. Here are some key points:
In summary, the solubility of 1-bromonaphthalen-2-ol is influenced by both its functional groups and the nature of the solvent. Remember, "like dissolves like," and this principle plays a crucial role in predicting and understanding the solubility behavior of this compound.