2-((2-Chloroethyl)sulphonyl)ethyl(2-((2-chloroethyl)sulphonyl)ethyl)ammonium chloride
2-[(2-chloroethyl)sulphonyl]ethyl[2-[(2-chloroethyl)sulphonyl]ethyl]ammonium chloride
CAS: 65180-91-8
Molecular Formula: C8H18Cl3NO4S2
2-((2-Chloroethyl)sulphonyl)ethyl(2-((2-chloroethyl)sulphonyl)ethyl)ammonium chloride - Names and Identifiers
| Name | 2-[(2-chloroethyl)sulphonyl]ethyl[2-[(2-chloroethyl)sulphonyl]ethyl]ammonium chloride |
| Synonyms | BIS[2-(2-CHLOROETHYLSULFONYL)ETHYL]AZANIUM CHLORIDE Bis[2-(2-chloroethyl)sulfonethyl]amine hydrochloride 2-[(2-chloroethyl)sulphonyl]ethyl[2-[(2-chloroethyl)sulphonyl]ethyl]ammonium chloride 2-[(2-chloroethyl)sulfonyl]-N-{2-[(2-chloroethyl)sulfonyl]ethyl}ethanaminium chloride 2-((2-Chloroethyl)sulphonyl)ethyl(2-((2-chloroethyl)sulphonyl)ethyl)ammonium chloride |
| CAS | 65180-91-8 |
| EINECS | 265-599-5 |
| InChI | InChI=1/C8H17Cl2NO4S2.ClH/c9-1-5-16(12,13)7-3-11-4-8-17(14,15)6-2-10;/h11H,1-8H2;1H |
2-((2-Chloroethyl)sulphonyl)ethyl(2-((2-chloroethyl)sulphonyl)ethyl)ammonium chloride - Physico-chemical Properties
| Molecular Formula | C8H18Cl3NO4S2 |
| Molar Mass | 362.72 |
| Boling Point | 585.9°C at 760 mmHg |
| Flash Point | 308.1°C |
| Vapor Presure | 1.04E-13mmHg at 25°C |
2-((2-Chloroethyl)sulphonyl)ethyl(2-((2-chloroethyl)sulphonyl)ethyl)ammonium chloride - Introduction
2-[(2-chlorophyll) sulphonyl]ethyl[2-[(2-chlorophyll) sulphonyl]ethyl]ammonium chloride is an organic compound with a chemical formula of C8H16Cl4N2O2S2 and a molecular weight of 335.15.
Nature:
-Appearance: Colorless or light yellow crystal powder
-Melting point: about 160-164°C
-Soluble: Soluble in water, methanol and ethanol, insoluble in ether
Use:
The compound can be widely used in chemical synthesis and organic synthesis reactions, including:
-As the main intermediate of anti-cancer drugs, it is used in the pharmaceutical industry to synthesize a variety of anti-tumor compounds
-Used as an intermediate in the synthesis of organic sulfur compounds
-for the synthesis of polypeptide compounds
Preparation Method:
2-[(2-chloroethyl)sulphonyl]ethyl[2-[(2-chloroethyl)sulphonyl]ethyl]ammonium The chloride synthesis method is relatively complex and usually needs to be carried out in a laboratory environment. A common method of preparation is by reaction of ethyl 2-chloroethanesulfonate and condensation reaction between 2-chloroethanesulfonyl chloride and diethylamine.
Safety Information:
-This compound may be irritating to the skin, eyes and respiratory tract
-Need to operate in a well-ventilated place
-After touching the skin, rinse with water immediately
-Use with appropriate chemical protective gloves, goggles and masks
-Avoid inhalation or ingestion of the compound
-Should be stored properly, away from fire and oxidizing agents
Nature:
-Appearance: Colorless or light yellow crystal powder
-Melting point: about 160-164°C
-Soluble: Soluble in water, methanol and ethanol, insoluble in ether
Use:
The compound can be widely used in chemical synthesis and organic synthesis reactions, including:
-As the main intermediate of anti-cancer drugs, it is used in the pharmaceutical industry to synthesize a variety of anti-tumor compounds
-Used as an intermediate in the synthesis of organic sulfur compounds
-for the synthesis of polypeptide compounds
Preparation Method:
2-[(2-chloroethyl)sulphonyl]ethyl[2-[(2-chloroethyl)sulphonyl]ethyl]ammonium The chloride synthesis method is relatively complex and usually needs to be carried out in a laboratory environment. A common method of preparation is by reaction of ethyl 2-chloroethanesulfonate and condensation reaction between 2-chloroethanesulfonyl chloride and diethylamine.
Safety Information:
-This compound may be irritating to the skin, eyes and respiratory tract
-Need to operate in a well-ventilated place
-After touching the skin, rinse with water immediately
-Use with appropriate chemical protective gloves, goggles and masks
-Avoid inhalation or ingestion of the compound
-Should be stored properly, away from fire and oxidizing agents
Last Update：2024-04-09 02:00:47
Supplier List
View History
2-((2-Chloroethyl)sulphonyl)ethyl(2-((2-chloroethyl)sulphonyl)ethyl)ammonium chloride
Boronic acid, B-[2-[(1-methylethyl)thio]-5-(trifluoromethyl)-3-pyridinyl]-
Carbamic acid, [2-(2-furanyl)ethenyl]-, (4-bromophenyl)methyl ester (9CI)
Prosapogenin C2
Acetic acid, 2-(3-ethyl-4-hydroxy-4-methyl-2-pyrrolidinylidene)-, ethyl ester
Pentacyclopentane-6-thiomethanol
Spiro[cyclohexane-1,4'(1'H)-isoquinoline]-1',3'(2'H)-dione, 2'-phenyl-
7-溴苯并噻吩
19-Norcholest-9-ene-3,6-diol,5-methyl-, diacetate, (3b,5b,6b)- (9CI)
Carbamic acid, dimethylthio-,O-[2-(methylthio)-4-pyrimidinyl] ester (8CI)
Boronic acid, B-[2-[(1-methylethyl)thio]-5-(trifluoromethyl)-3-pyridinyl]-
Carbamic acid, [2-(2-furanyl)ethenyl]-, (4-bromophenyl)methyl ester (9CI)
Prosapogenin C2
Acetic acid, 2-(3-ethyl-4-hydroxy-4-methyl-2-pyrrolidinylidene)-, ethyl ester
Pentacyclopentane-6-thiomethanol
Spiro[cyclohexane-1,4'(1'H)-isoquinoline]-1',3'(2'H)-dione, 2'-phenyl-
7-溴苯并噻吩
19-Norcholest-9-ene-3,6-diol,5-methyl-, diacetate, (3b,5b,6b)- (9CI)
Carbamic acid, dimethylthio-,O-[2-(methylthio)-4-pyrimidinyl] ester (8CI)