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2-Bromopropene

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Identification
Molecular formula
C3H5Br
CAS number
557-93-7
IUPAC name
2-bromoprop-1-ene
State
State

At room temperature, 2-Bromopropene is in a liquid state. It is typically handled with care due to its reactive nature as an alkyl halide.

Melting point (Celsius)
-142.50
Melting point (Kelvin)
130.65
Boiling point (Celsius)
59.00
Boiling point (Kelvin)
332.15
General information
Molecular weight
120.98g/mol
Molar mass
120.9870g/mol
Density
1.3116g/cm3
Appearence

2-Bromopropene is a colorless to light yellow liquid. It is an organobromine compound that emits a sharp, pungent odor.

Comment on solubility

Solubility of 2-bromoprop-1-ene

2-bromoprop-1-ene, with the chemical formula C3H5Br, exhibits some interesting solubility characteristics that highlight the influence of its molecular structure on its behavior in different solvents.

In general, the solubility of 2-bromoprop-1-ene can be summarized as follows:

  • This compound is relatively insoluble in water, which can be attributed to its non-polar characteristics and the presence of the bromine atom.
  • However, it demonstrates good solubility in organic solvents such as ethanol, acetone, and other non-polar solvents, making it suited for various organic reactions.
  • As a result of this behavior, 2-bromoprop-1-ene is often used in organic synthesis, particularly in reactions where a non-polar environment is required.

In conclusion, the solubility of 2-bromoprop-1-ene emphasizes the importance of both molecular structure and the nature of the solvent used. As a general rule of thumb, like dissolves like, meaning that polar solvents are unlikely to solubilize non-polar compounds effectively.

Interesting facts

Interesting Facts about 2-Bromoprop-1-ene

2-Bromoprop-1-ene is a fascinating organobromine compound that serves as an important intermediate in various chemical reactions and applications. Some intriguing facts about this compound include:

  • Structural Characteristics: 2-Bromoprop-1-ene features a bromine atom attached to the second carbon of the propene chain, influencing its reactivity and properties.
  • Reactivity: This compound is known for undergoing typical electrophilic addition reactions, which can lead to the formation of a variety of other organic compounds, making it useful in synthetic organic chemistry.
  • Application in Synthesis: It serves as a key building block in the synthesis of herbicides, pharmaceuticals, and other agrochemicals, demonstrating its significance in agriculture and medicine.
  • Chirality and Stereochemistry: Although 2-bromoprop-1-ene itself is not chiral, its derivatives can exhibit chirality, opening up avenues for stereochemical studies and chiral synthesis.
  • Environmental Considerations: The presence of bromine in this compound can pose environmental challenges, prompting research into more sustainable alternatives and methods for its safe use.

As a compound integral to various synthetic pathways, 2-bromoprop-1-ene exemplifies how specific functional groups and molecular structures can dramatically influence chemical behavior and application.

Synonyms
2-BROMOPROPENE
2-bromoprop-1-ene
1-Propene, 2-bromo-
2-Bromo-1-propene
C8GT7P5ZZS
EINECS 209-185-4
BRN 1731926
CH3CBr=CH2
NSC-87535
DTXSID8060325
4-01-00-00754 (Beilstein Handbook Reference)
2bromopropene
2Bromopropylene
Propene, 2bromo
1Propene, 2bromo
alphaMethylvinyl bromide
DTXCID4041945
209-185-4
inchi=1/c3h5br/c1-3(2)4/h1h2,2h
phmrpwpddrgggf-uhfffaoysa-n
un1993
557-93-7
Isopropenyl bromide
2-Bromopropylene
Isopropylene bromide
Propene, 2-bromo-
NSC 87535
.alpha.-Methylvinyl bromide
alpha-Methylvinyl bromide
2-Bromopropene, 99%
MFCD00000140
2-Bromo-propene
2-bromanylprop-1-ene
UNII-C8GT7P5ZZS
SCHEMBL270208
NSC87535
CCG-40506
AKOS015968899
FS-4260
DB-000140
B1269
NS00033395
EN300-72133
A815309
213972-86-2