Interesting facts
Interesting Facts about 2-Bromoacetic Acid
2-Bromoacetic acid is a fascinating compound that holds significant value in various fields of chemistry and industry. Here are some intriguing aspects of this compound:
- Structural Importance: 2-Bromoacetic acid is a halogenated derivative of acetic acid, where the Br (bromine) atom is positioned at the second carbon atom. This modification can markedly influence the compound’s reactivity and properties.
- Reactivity: The presence of the bromine atom makes 2-bromoacetic acid a useful reagent in organic synthesis. It can participate in nucleophilic substitution reactions, allowing chemists to introduce various functional groups into organic molecules.
- Biological Relevance: This compound is utilized in biochemical research, particularly in the study of enzyme mechanisms and metabolic pathways. Its ability to modify biomolecules can lead to insightful discoveries in medicinal chemistry.
- Toxicity: While 2-bromoacetic acid has valuable applications, it is important to note that it can be toxic and must be handled with caution. Awareness of its hazardous nature is crucial in laboratory settings.
- Applications: Beyond research, this compound finds its place in the production of pharmaceuticals, agrochemicals, and other chemical intermediates. Its functional properties make it beneficial in various applications.
As a compound, 2-bromoacetic acid demonstrates how subtle changes in molecular structure can lead to dramatic shifts in chemical behavior and utility. Whether in a laboratory or an industrial context, this bromoacetic derivative exemplifies the importance of understanding chemical structure in relation to function.
Synonyms
BROMOACETIC ACID
2-Bromoacetic acid
79-08-3
Acetic acid, bromo-
Monobromoacetic acid
Bromoethanoic acid
To NTU
Bromoacetate ion
Acide bromacetique
2-Bromoacetyl Group
Acetic acid, 2-bromo-
2-bromoethanoic acid
Bromo-acetic acid
Monobromessigsaeure
Kyselina bromoctova
alpha-Bromoacetic acid
Caswell No. 112A
.alpha.-Bromoacetic acid
NSC 141
Acide bromacetique [French]
Kyselina bromoctova [Czech]
Monobromessigsaeure [German]
CCRIS 7886
Bromoacetic acid, solid
EINECS 201-175-8
UN1938
Carboxymethyl bromide
EPA Pesticide Chemical Code 008702
BRN 0506167
CH2BrCOOH
DTXSID7021495
AI3-15301
HSDB 7627
NSC-141
MFCD00002678
2B3HS32431
BROMOACETIC ACID [MI]
BROMOACETIC ACID, 2-
CHEMBL60851
DTXCID601495
BROMOACETIC ACID [HSDB]
EC 201-175-8
4-02-00-00526 (Beilstein Handbook Reference)
BROMOACETIC ACID, (SOLID)
BROMOACETIC ACID, [SOLID]
alpha-Bromoethanoic acid
2-Bromoaceticacid
bromacetic acid
BROMOACETIC ACID, PRACT
UNII-2B3HS32431
2bromoacetic acid
bromo acetic acid
a-bromoacetic acid
monobromacetic acid
acetic acid, bromo
a-Bromoethanoic acid
alphaBromoacetic acid
UN3425
2-bromo acetic acid
2-bromo-acetic acid
Acetic acid, 2bromo
alphaBromoethanoic acid
UN 1938
2-bromanylethanoic acid
44 - Haloacetic Acids
.alpha.-Bromoethanoic acid
WLN: QV1E
SCHEMBL23032
Bromoacetic acid, solid (dot)
NSC141
Bromoacetic acid solution (dot)
Acetic acid, bromo, (solution)
Bromoacetic acid (acd/name 4.0)
STR00860
Tox21_200657
BDBM50119693
Bromoacetic acid, analytical standard
LMFA01090074
STL481895
AKOS000118919
Bromoacetic acid, reagent grade, 97%
DB02198
FB01815
MSK70014-1000Q
CAS-79-08-3
NCGC00091467-01
NCGC00091467-02
NCGC00258211-01
BP-20544
FB181790
Bromoacetic acid, purum, >=98.0% (T)
Bromoacetic acid, ReagentPlus(R), >=99%
B0531
NS00010208
Bromoacetic acid, ReagentPlus(R), >=99.0%
EN300-19170
Bromoacetic acid Solution in MTBE, 1000ug/mL
G77237
Bromoacetic acid, solid [UN1938] [Corrosive]
A839576
Q421323
F2191-0223
Z104473018
Bromoacetic acid 1000 microg/mL in Methyl-tert-butyl ether
201-175-8
Solubility of 2-bromoacetic acid
2-bromoacetic acid (C2H3BrO2) exhibits notable solubility characteristics that make it interesting for various applications. Here are some key points regarding its solubility:
Overall, the solubility of 2-bromoacetic acid is a significant factor that influences its behavior in chemical processes and its interactions within various environments.