2-CHLORO-1,3-DIMETHYLAMINO TRIMETHINIUM HEXAFLUOROPHOSPHATE
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate
CAS: 291756-76-8
Molecular Formula: C7H14ClF6N2P
2-CHLORO-1,3-DIMETHYLAMINO TRIMETHINIUM HEXAFLUOROPHOSPHATE - Names and Identifiers
2-CHLORO-1,3-DIMETHYLAMINO TRIMETHINIUM HEXAFLUOROPHOSPHATE - Physico-chemical Properties
| Molecular Formula | C7H14ClF6N2P |
| Molar Mass | 306.62 |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
2-CHLORO-1,3-DIMETHYLAMINO TRIMETHINIUM HEXAFLUOROPHOSPHATE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| WGK Germany | 3 |
2-CHLORO-1,3-DIMETHYLAMINO TRIMETHINIUM HEXAFLUOROPHOSPHATE - Introduction
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
-Chemical formula: C8H16ClF6N2P
-Molecular weight: 330.636g/mol
-Appearance: Colorless crystalline solid
-Melting point: 140-142°C
-Soluble: Soluble in water and many organic solvents
Use:
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate has a wide range of applications in organic synthesis and catalytic reactions. It is commonly used as a nucleophile and catalyst, participating in different types of reactions, such as: Micheal addition, Mannich reaction, Aldol reaction, nucleophilic substitution reaction, etc. Because of its excellent nucleophilicity, it plays an important role in the synthesis of organic molecules and drugs.
Preparation Method:
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate are generally synthesized by the following steps:
1. take 2-chloro -3-dimethylamino-propenal and methyl amine reaction, generate N,N-dimethyl -3-dimethylamino acrylamide.
2. In the presence of hydrogen chloride, N, N-dimethyl-3-dimethylaminoacrylamide is reacted with butyric anhydride to generate-(2-chloro-3-dimethylamino-2-propenyl)-dimethylamine.
3. The above product is reacted with hexafluorophosphoric acid to generate the final product (2-chloro -3-dimethylamino -2-propenyl)-dimethyl ammonium hexafluorophosphate.
Safety Information:
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate is a chemical and should be disposed of properly. Here are some safety considerations:
-Wear protective gloves, safety glasses and protective clothing when using.
-Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water.
-Use under well-ventilated conditions to avoid inhaling gas or solution vapor.
-Avoid contact with acids, oxidizing agents or flammable substances, and keep away from open flames and high temperatures.
-If ingested or inhaled, seek medical attention and provide information immediately.
Nature:
-Chemical formula: C8H16ClF6N2P
-Molecular weight: 330.636g/mol
-Appearance: Colorless crystalline solid
-Melting point: 140-142°C
-Soluble: Soluble in water and many organic solvents
Use:
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate has a wide range of applications in organic synthesis and catalytic reactions. It is commonly used as a nucleophile and catalyst, participating in different types of reactions, such as: Micheal addition, Mannich reaction, Aldol reaction, nucleophilic substitution reaction, etc. Because of its excellent nucleophilicity, it plays an important role in the synthesis of organic molecules and drugs.
Preparation Method:
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate are generally synthesized by the following steps:
1. take 2-chloro -3-dimethylamino-propenal and methyl amine reaction, generate N,N-dimethyl -3-dimethylamino acrylamide.
2. In the presence of hydrogen chloride, N, N-dimethyl-3-dimethylaminoacrylamide is reacted with butyric anhydride to generate-(2-chloro-3-dimethylamino-2-propenyl)-dimethylamine.
3. The above product is reacted with hexafluorophosphoric acid to generate the final product (2-chloro -3-dimethylamino -2-propenyl)-dimethyl ammonium hexafluorophosphate.
Safety Information:
(Z)-N-[2-Chloro-3-(dimethylamino)allylidene]-N-methylmethanaminium Hexafluorophosphate is a chemical and should be disposed of properly. Here are some safety considerations:
-Wear protective gloves, safety glasses and protective clothing when using.
-Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water.
-Use under well-ventilated conditions to avoid inhaling gas or solution vapor.
-Avoid contact with acids, oxidizing agents or flammable substances, and keep away from open flames and high temperatures.
-If ingested or inhaled, seek medical attention and provide information immediately.
Last Update：2024-04-09 02:00:49
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Tel: +86-18821248368
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View History
2-CHLORO-1,3-DIMETHYLAMINO TRIMETHINIUM HEXAFLUOROPHOSPHATE
Methyl hexanoate, 6-hydroxy-hexanoate
碘化三甲基·全氟辛基磺酰胺丙基铵
乙酰基-3-(2-萘基)丙氨酸
OTAVA-BB BB7211740014
3-(2,2-二氯乙烯基)-2,2-二甲基环丙基羧酸甲基酯
25 MG CALPAIN INHIBITOR IIRESEARCH GRADE
3-METHACRYLOXYPROPYLDIMETHYLETHOXYSILANE INHIBITED
Scopoline Methobromide (Tiotropium Bromide Impurity H)
印八角枫林碱
Methyl hexanoate, 6-hydroxy-hexanoate
碘化三甲基·全氟辛基磺酰胺丙基铵
乙酰基-3-(2-萘基)丙氨酸
OTAVA-BB BB7211740014
3-(2,2-二氯乙烯基)-2,2-二甲基环丙基羧酸甲基酯
25 MG CALPAIN INHIBITOR IIRESEARCH GRADE
3-METHACRYLOXYPROPYLDIMETHYLETHOXYSILANE INHIBITED
Scopoline Methobromide (Tiotropium Bromide Impurity H)
印八角枫林碱