CAS 249561-98-6

Methanaminium, N-[2-chloro-3-(dimethylamino)-2-propen-1-ylidene]-N-methyl-, hexafluorophosphate(1-) (1:1)

Description:

Methanaminium, N-[2-chloro-3-(dimethylamino)-2-propen-1-ylidene]-N-methyl-, hexafluorophosphate(1-) (1:1), commonly referred to by its CAS number 249561-98-6, is an organic compound characterized by its quaternary ammonium structure. This substance features a methanaminium core substituted with a chloro and a dimethylamino group, contributing to its unique reactivity and properties. The presence of the hexafluorophosphate anion indicates strong ionic interactions, which can enhance solubility in polar solvents and influence its stability. Typically, compounds of this nature are utilized in various applications, including as ionic liquids or in electrochemical systems, due to their ability to conduct electricity and their thermal stability. The specific arrangement of substituents on the methanaminium moiety can also impart distinct biological or chemical activities, making it of interest in fields such as medicinal chemistry or materials science. Overall, this compound exemplifies the diverse functionalities that can arise from quaternary ammonium salts.

Formula: C₇H₁₄ClN₂·F₆P

InChI: InChI=1S/C7H14ClN2.F6P/c1-9(2)5-7(8)6-10(3)4;1-7(2,3,4,5)6/h5-6H,1-4H3;/q+1;-1

InChI key: InChIKey=PIUHAULDXSPPQV-UHFFFAOYSA-N

SMILES: C(C(=CN(C)C)Cl)=[N+](C)C.[P+5]([F-])([F-])([F-])([F-])([F-])[F-]

Synonyms:

• CDT Phosphate
• Methanaminium, N-[2-chloro-3-(dimethylamino)-2-propen-1-ylidene]-N-methyl-, hexafluorophosphate(1-) (1:1)
• Methanaminium, N-[2-chloro-3-(dimethylamino)-2-propenylidene]-N-methyl-, hexafluorophosphate(1-)

Methanaminium, N-[2-chloro-3-(dimethylamino)-2-propen-1-ylidene]-N-methyl-, hexafluorophosphate(1-) (1:1)

CAS: 249561-98-6

Formula: C₇H₁₄ClF₆N₂P

Purity: 97%

Color and Shape: Solid

Molecular weight: 306.6166

Ref: IN-DA002PZ8

Methanaminium, N-[2-chloro-3-(dimethylamino)-2-propen-1-ylidene]-N-methyl-, hexafluorophosphate(1-) (1:1)

CAS: 249561-98-6

Methanaminium, N-[2-chloro-3-(dimethylamino)-2-propen-1-ylidene]-N-methyl-, hexafluorophosphate(1-) (1:1)

Purity: 97%

Molecular weight: 306.62g/mol

Ref: 54-PC1002169

2-Chloro-1,3-bis(dimethylamino)trimethinium Hexafluorophosphate

CAS: 249561-98-6

Formula: C₇H₁₄ClN₂·F₆P

Color and Shape: Neat

Molecular weight: 306.62

Ref: 86-MM0965.03

Etoricoxib Impurity 65

CAS: 249561-98-6

Formula: C₇H₁₄ClF₆N₂P

Molecular weight: 306.62

Ref: 4Z-E-4571

Etoricoxib Impurity 41

CAS: 249561-98-6

Formula: C₇H₁₄ClN₂F₆P

Molecular weight: 161.65 : 144.96

Ref: ST-EA-CP-E1009

N-[2-Chloro-3-(dimethylamino)-2-propen-1-ylidene]-N-methylmethanaminium Hexafluorophosphate

CAS: 249561-98-6

Formula: C₇H₁₄ClN₂·F₆P

Color and Shape: White To Light Yellow

Molecular weight: 306.62

Ref: TR-C293325

2-Chloro-1,3-bis(dimethylamino)trimethinium hexafluorophosphate

CAS: 249561-98-6

2-Chloro-1,3-bis(dimethylamino)trimethinium hexafluorophosphate is a glycogen phosphorylase inhibitor. It is a synthetic compound that belongs to the class of allylamines. The synthesis of 2-chloro-1,3-bis(dimethylamino)trimethinium hexafluorophosphate has been achieved by reacting phosphorus oxychloride with dimethylformamide and amines. This reaction leads to the formation of chlorides and heterocycles. 2-Chloro-1,3-bis(dimethylamino)trimethinium hexafluorophosphate inhibits glycogen phosphorylase by binding to the active site and blocking access to the substrate glucose. It also inhibits β-glucosidase, which prevents the hydrolysis of glucosides into glucose.

Formula: C₇H₁₄ClN₂·PF₆

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 306.62 g/mol

Ref: 3D-FC35481

N-(2-Chloro-3-(dimethylamino)allylidene)-N-methylmethanaminium hexafluorophosphate(V)

CAS: 249561-98-6

Formula: C₇H₁₄ClF₆N₂P

Purity: 95%

Color and Shape: Solid

Molecular weight: 306.62

Ref: 10-F449689