Skip to main content

Thiamethoxam

ADVERTISEMENT
Identification
Molecular formula
C8H10ClN5O3S
CAS number
153719-23-4
IUPAC name
N1'-[2-[[2-[(dimethylamino)methyl]thiazol-4-yl]methylsulfanyl]ethyl]-N1-methyl-2-nitro-ethene-1,1-diamine
State
State

At room temperature, thiamethoxam is typically found in a solid state.

Melting point (Celsius)
139.10
Melting point (Kelvin)
412.25
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
291.71g/mol
Molar mass
291.7140g/mol
Density
1.5700g/cm3
Appearence

Thiamethoxam is typically found in the form of colorless crystals. However, it can also appear as a beige to brown powder.

Comment on solubility

Solubility of N1'-[2-[[2-[(dimethylamino)methyl]thiazol-4-yl]methylsulfanyl]ethyl]-N1-methyl-2-nitro-ethene-1,1-diamine

The compound N1'-[2-[[2-[(dimethylamino)methyl]thiazol-4-yl]methylsulfanyl]ethyl]-N1-methyl-2-nitro-ethene-1,1-diamine, with the chemical formula C8H10ClN5O3S, exhibits a nuanced solubility profile that can be influenced by its structure.

Factors Affecting Solubility

The solubility of this compound can be assessed based on several factors:

  • Polarity: The presence of polar functional groups (such as nitro and amine groups) enhances the solubility in polar solvents like water.
  • Hydrophobicity: The thiazole and dimethylamino groups may contribute to hydrophobic characteristics, making it more soluble in organic solvents.
  • Ionization: The potential for ionization in aqueous environments can dramatically affect solubility, especially for amines.

General Observations

It is commonly observed that:

  • Compounds similar to this one often show limited solubility in cold water but may dissolve better in warm aqueous solutions.
  • Organics, such as ethanol or DMSO, can effectively dissolve this compound due to their ability to interact with various polar and non-polar segments.
  • In the presence of acids, the compound might become more soluble due to protonation of the amine groups.

In conclusion, the solubility of N1'-[2-[[2-[(dimethylamino)methyl]thiazol-4-yl]methylsulfanyl]ethyl]-N1-methyl-2-nitro-ethene-1,1-diamine is contingent on its chemical environment and the solvent used, which warrants careful consideration in applications requiring dissolution.

Interesting facts

Exploring the Compound: N1'-[2-[[2-[(dimethylamino)methyl]thiazol-4-yl]methylsulfanyl]ethyl]-N1-methyl-2-nitro-ethene-1,1-diamine

This intriguing compound, known for its complex structure, opens up a world of potential applications and chemical behaviors. Here are some fascinating insights:

  • Unique Structure: The compound features a thiazole ring, which is a five-membered heterocycle containing sulfur and nitrogen. This makes it chemically diverse and reactive, ideal for various organic synthesis reactions.
  • Biological Activity: Compounds with similar structural characteristics have been explored for their biological activities, including antimicrobial and anticancer properties. Its interaction with biological systems could prove essential for developing new therapeutic agents.
  • Dimethylamino Group: The presence of a dimethylamino group indicates potential in acting as a base and forming complexes with acids or other electrophiles, enhancing its reactivity and application in drug formulation.
  • Nitro Group: The nitro group adds to the compound's electrophilic character, often involved in nucleophilic substitution reactions. This property can be harnessed in synthesizing more complex chemical entities.
  • Potential Research Avenues: Given its diverse functional groups, chemical scientists can explore various research avenues such as:
    • Medicinal chemistry for developing new drug candidates.
    • Studying its mechanism of action in biological systems.
    • Investigating its application in material sciences.

The compound's rich functional group array not only makes it a subject of study within laboratories but also highlights its potential in innovative chemical applications. As each component interacts within a larger system, understanding the compound's behavior will pave the way for future discoveries.

Synonyms
Acinon
Nizatidina
Axid Ar
Nizatidinum
P41PML4GHR
Axid
LY 139037
NSC-759289
CHEBI:7601
DTXSID5023376
NIZATIDINE (MART.)
NIZATIDINE [MART.]
NIZATIDINE (USP-RS)
NIZATIDINE [USP-RS]
Zanizal
1,1-Ethenediamine, N-(2-(((2-((dimethylamino)methyl)-4-thiazolyl)methyl)thio)ethyl)-N'-methyl-2-nitro-
N-(2-(((2-((Dimethylamino)methyl)-4-thiazolyl)methyl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine
Nizax
LY-139037
NIZATIDINE (EP MONOGRAPH)
NIZATIDINE (USP IMPURITY)
NIZATIDINE [EP MONOGRAPH]
NIZATIDINE [USP IMPURITY]
NIZATIDINE (USP MONOGRAPH)
NIZATIDINE [USP MONOGRAPH]
DTXCID403376
Antizid
Distaxid
Galitidin
Gastrax
Naxidine
Nizaxid
Panaxid
Ulcosol
Ulxid
Zinga
MFCD00865660
ZE-101
ZL-101
Splendil ER
n-[2-[[[2-[(dimethylamino)methyl]-4-thiazolyl]methyl]thio]ethyl]-n'-methyl-2-nitro-1,1-ethenediamine
Nizatidinum [Latin]
Nizatidina [Spanish]
NIZATIDINE [MI]
NIZATIDINE [INN]
NIZATIDINE [JAN]
Prestwick0_000921
Prestwick1_000921
UNII-P41PML4GHR
NIZATIDINE [HSDB]
NIZATIDINE [USAN]
1,1-Ethenediamine, N-
NIZATIDINE [VANDF]
NIZATIDINE [WHO-DD]
SPBio_003001
CHEMBL3183075
NIZATIDINE [ORANGE BOOK]
HSDB 3574
A02BA04
SGXXNSQHWDMGGP-UHFFFAOYSA-N
HMS1570J04
HMS3373M20
HMS3374E07
HMS3393K04
HMS3651C04
BCP06707
AKOS037515490
Nizatidine [USAN:USP:INN:BAN:JAN]
NSC 759289
BRN 4846056
SY077303
N0933
1,1-Ethenediamine, N-(2-(((2-((dimethylamino)methyl)-4-thiazoly)methyl)thio)ethyl)-N'-methyl-2-nitro-
N-(2-(((2-((DIMETHYLAMINO)METHYL)-4-THIAZOLYL)METHYL)THIO)ETHYL)-N'-METHYL-2-NITRO-1,1-ETHENE DIAMINE
N-(4-(6-Methylamino-7-nitro-2-thia-5-aza-6-hepten-1-yl)-2-thiazolylmethyl)-N,N-dimethylamin
N-[2-[[[2-[(Dimethylamino)methyl]-4-thiazolyl]methyl]thio]ethyl]-N inverted exclamation mark -methyl-2-nitroethene-1,1-diamine
N-methyl-N'-[2-(2-dimethylaminomethylthiazol-4-ylmethylthio)ethyl]-2-nitro-1,1-ethenediamine