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Saclofen

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Identification
Molecular formula
C8H7NO3S
CAS number
149866-51-7
IUPAC name
2-methyl-1,1-dioxo-1,2-benzothiazol-3-one
State
State

At room temperature, Saclofen is typically in a solid state.

Melting point (Celsius)
147.00
Melting point (Kelvin)
420.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
215.25g/mol
Molar mass
215.2510g/mol
Density
1.7080g/cm3
Appearence

Saclofen appears as a white to off-white solid at room temperature.

Comment on solubility

Solubility of 2-methyl-1,1-dioxo-1,2-benzothiazol-3-one

The solubility of 2-methyl-1,1-dioxo-1,2-benzothiazol-3-one (C8H7NO2S) presents interesting characteristics worth noting. This compound is a member of the benzothiazole class, which often exhibit varied solubility behavior based on structural factors and interactions with solvents.

Here are some key points regarding its solubility:

  • Polarity: The presence of the dioxo group contributes to certain polar characteristics. Thus, 2-methyl-1,1-dioxo-1,2-benzothiazol-3-one may be soluble in polar solvents.
  • Temperature dependency: Solubility can increase with temperature in many cases, so the conditions under which this compound is dissolved are significant.
  • Practical applications: Knowing the solubility aids in determining suitable solvents for reactions or formulations involving this compound.

Despite its potential solubility in polar solvents, it's essential to conduct empirical testing to pinpoint exact solubility values. Note that varying substituents and their positions can significantly influence the solubility behavior of these compounds.

As always, solubility is a crucial parameter in the formulation and application, making it a vital factor in research and industrial contexts.

Interesting facts

Exploring 2-methyl-1,1-dioxo-1,2-benzothiazol-3-one

2-methyl-1,1-dioxo-1,2-benzothiazol-3-one, also known by its more common name Benzothiazolone, is a fascinating compound that plays an essential role in various fields, particularly in organic chemistry and material science. Here are some key facts about this intriguing compound:

  • Versatility in Applications: Benzothiazolone derivatives are widely used in the manufacture of dyes, pigments, and fluorescent brighteners. Their unique structure allows them to impart vivid colors to textiles and plastics.
  • Biological Significance: Some studies suggest that compounds in this class may exhibit antibacterial and antifungal properties, making them potential candidates in pharmaceuticals for treating infections.
  • Environmental Impact: Given its usage in various industrial applications, researchers are continuously exploring the environmental impact of this compound, leading to the development of safer alternatives.
  • Synthetic Pathways: The synthesis of Benzothiazolone is a topic of interest among chemists. Researchers have developed several methods for its production, often focusing on enhancing yield and minimizing waste.
  • Intrinsic Properties: This compound features a unique dioxo group, enhancing its reactivity and interactions. This structural characteristic makes it a prime subject for studying reaction mechanisms in organic chemistry.

As you delve deeper into the world of 2-methyl-1,1-dioxo-1,2-benzothiazol-3-one, you’ll discover a compound that is not only essential in industrial processes but also a potential player in the innovation of new materials and therapeutics. Its ongoing research promises to unveil even more intriguing applications and properties!

Synonyms
2-Methyl-1,2-benzisothiazol-3(2H)-one 1,1-dioxide
N-Methylsaccharin
15448-99-4
2-Methylbenzo[d]isothiazol-3(2H)-one 1,1-dioxide
2-methyl-1,1-dioxo-1,2-benzothiazol-3-one
MFCD00059263
NSC 39120
T63VBY3AYH
CHEMBL131790
2-methyl-1,2-benzothiazol-3(2H)-one 1,1-dioxide
NSC-39120
1,2-Benzisothiazolin-3-one, 2-methyl-, 1,1-dioxide
2-Methyl-1,2-benzisothiazole-3(2H)-one-1,1-dioxide
1,2-Benzisothiazol-3(2H)-one, 2-methyl-, 1,1-dioxide
UNII-T63VBY3AYH
Methylsaccharin
methyl saccharine
NSC39120
EINECS 239-466-7
AI3-23674
2-Methyl-1,1-dioxide
triflusulfuron-methyl TP1
SCHEMBL107126
SCHEMBL30339085
1, 2-methyl-, 1,1-dioxide
DTXSID10165639
BDBM50496471
STL293362
AKOS016011169
DS-6404
SY053783
DB-007773
CS-0151203
M0427
NS00025020
2-methyl-1,1-dioxo-benzo[d]isothiazol-3-one
D78426
Q27289719
2-methyl-2,3-dihydro-1,2-benzothiazole-1,1,3-trione
2-methyl-2,3-dihydro-1lambda,2-benzothiazole-1,1,3-trione
2-Methyl-1,1-dioxo-1,2-dihydro-1lambda*6*-benzo[d]isothiazol-3-one