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2,4-Dichlorobenzyl alcohol

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Identification
Molecular formula
C7H6Cl2O
CAS number
1777-82-8
IUPAC name
(2,4-dichlorophenyl)methanol
State
State

At room temperature, 2,4-Dichlorobenzyl alcohol is primarily found in a solid state. It retains its structure under typical room conditions and does not evaporate easily, reflecting its relatively high boiling point compared to some other benzyl alcohol derivatives.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
177.03g/mol
Molar mass
177.0270g/mol
Density
1.4380g/cm3
Appearence

2,4-Dichlorobenzyl alcohol typically appears as a white to off-white crystalline solid. It is often found in powder form or as small solid granules. Due to its purity, it may also appear translucent under certain lighting conditions. It has no significant odor, which makes it distinct from some other aromatic compounds.

Comment on solubility

Solubility of (2,4-Dichlorophenyl)methanol

(2,4-Dichlorophenyl)methanol, also known by its IUPAC name, is an organic compound that presents unique solubility characteristics. Understanding its solubility can be approached through several factors:

  • Polar and Nonpolar Interactions: Due to the presence of a hydroxyl group (-OH) in its structure, (2,4-Dichlorophenyl)methanol exhibits polar characteristics. This leads to stronger interactions with polar solvents such as water.
  • Solvation: The ability of (2,4-Dichlorophenyl)methanol to form hydrogen bonds enhances its solubility in polar solvents. This can be particularly crucial in applications requiring solvation.
  • Solubility in Organic Solvents: While it is soluble in water, (2,4-Dichlorophenyl)methanol is also soluble in various organic solvents, such as ethanol and acetone, due to its partially nonpolar aromatic structure.

In contrast, its solubility in nonpolar solvents is generally low. In summary, one could quote, “The solubility of (2,4-Dichlorophenyl)methanol is a balance between its polar and nonpolar characteristics, allowing it to dissolve well in both polar and moderately nonpolar environments.”

This duality in solubility opens up various avenues for its use in chemical applications and formulations.

Interesting facts

Interesting Facts about (2,4-Dichlorophenyl)methanol

(2,4-Dichlorophenyl)methanol, also known as a key derivative of phenolic compounds, presents a fascinating study area for chemists and students alike. This compound plays an important role in various applications due to its unique chemical structure and properties.

Notable Applications

  • Pharmaceuticals: As a precursor in the synthesis of numerous pharmaceuticals, (2,4-dichlorophenyl)methanol aids in the development of medications that combat a variety of ailments.
  • Agricultural Chemicals: Its reactivity makes it valuable in producing herbicides and pesticides, thus enhancing agricultural productivity.
  • Industrial Uses: This compound is employed in the manufacture of plastics and dyes, showcasing its versatility in diverse industries.

Chemical Properties

This compound is characterized by the presence of two chlorine atoms positioned ortho and para to the hydroxymethyl group. This specific arrangement results in:

  • Increased stability: The chlorinated phenyl groups provide additional stabilization to the compound.
  • Enhanced reactivity: The functional groups can participate in various chemical reactions, including electrophilic substitutions.

Research Significance

Researchers often explore (2,4-dichlorophenyl)methanol for its potential in developing new materials and its environmental impact. Some key points of research include:

  • Investigating its role as an intermediate in organic synthesis.
  • Assessing its toxicity and environmental persistence, ensuring safety in its applications.

In summary, (2,4-dichlorophenyl)methanol is not just a simple compound but a significant entity in the world of chemistry. Its diverse applications, intriguing chemical properties, and ongoing research make it an essential subject for further study and exploration.

Synonyms
2,4-Dichlorobenzyl alcohol
1777-82-8
(2,4-Dichlorophenyl)methanol
Dichlorobenzyl alcohol
2,4-Dichlorobenzenemethanol
EINECS 217-210-5
NSC 15635
NSC-15635
UNII-1NKX3648J9
BRN 1448652
DTXSID9041362
AI3-20619
1NKX3648J9
DTXCID7021362
DICHLOROBENZYL ALCOHOL [II]
DICHLOROBENZYL ALCOHOL [MI]
DICHLOROBENZYL ALCOHOL [VANDF]
DICHLOROBENZYL ALCOHOL [MART.]
DICHLOROBENZYL ALCOHOL [WHO-DD]
2,4-DICHLOROBENZYL ALCOHOL [EP MONOGRAPH]
DICHLOROBENZYL ALCOHOL (II)
DICHLOROBENZYL ALCOHOL (MART.)
2,4-DICHLOROBENZYL ALCOHOL (EP MONOGRAPH)
Alcohol diclorobencilico
DTXCID2075346
DICHLOROBENZYL ALCOHOL [INCI]
4-06-00-02597 (beilstein handbook reference)
bayer 4245
dbhodfsfbxjzny-uhfffaoysa-n
dtxsid40152855
inchi=1/c7h6cl2o/c8-6-2-1-5(4-10)7(9)3-6/h1-3,10h,4h
Dybenal
Rapidosept
Benzenemethanol, 2,4-dichloro-
Myacide SP
Benzyl alcohol, 2,4-dichloro-
MFCD00004606
CHEBI:48220
NCGC00181337-01
CAS-1777-82-8
2,4-DICHLOROBENZYLALCOHOL
benzylalcohol,2,4-dichloro-
SCHEMBL41323
CHEMBL3184437
(2,4-Dichlorophenyl)methanol #
DAlc2-H_000039
2,4-Dichlorobenzyl alcohol, 99%
HY-W039454R
NSC15635
Tox21_112796
Tox21_300895
BDBM50498198
s6067
STL480884
AKOS000248902
Tox21_112796_1
2,4-Dichlorobenzyl alcohol (Standard)
DB13269
FD07106
HY-W039454
PS-5315
NCGC00181337-02
NCGC00181337-03
NCGC00254799-01
AC-10679
SY015811
DB-015914
CS-0097299
D1837
NS00003371
EN300-97623
A10326
SBI-0653934.0001
Q209202
SR-01000944729
SR-01000944729-1
Z111479786
2,4-Dichlorobenzyl alcohol, European Pharmacopoeia (EP) Reference Standard