5776-49-8

Basic information

• Product Name: Phosphoramide mustard cyclohexamine salt
• Synonyms: Phosphoramide mustard cyclohexamine salt;N,N-Bis(2-chloroethyl)phosphorodiamidic acid, cyclohexylammonium salt;Omf 59;Phosphorodiamidic acid, N,N-bis(2-chloroethyl)-, compd. with cyclohexanamine (1:1);Phosphorodiamidic acid, N,N-bis(2-chloroethyl)-, compd. with cyclohexylamine (1:1);Phosphorodiamidic acid, N,N-bis(2-chloroethyl)-, cyclohexylamine salt;N,N-Bis(2-chloroethyl)phosphorodiamidic acid - cyclohexanamine (1:1)
• CAS NO: 5776-49-8
• Molecular Formula: C4H11Cl2N2O2P•C6H13N
• Molecular Weight: 320.24
• Mol File: 5776-49-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 363.5°Cat760mmHg
• Flash Point: 173.6°C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: Phosphoramide mustard cyclohexamine salt(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphoramide mustard cyclohexamine salt(5776-49-8)
• EPA Substance Registry System: Phosphoramide mustard cyclohexamine salt(5776-49-8)

Safety Data

• Safety Statements: 3, Cl−, POx, and NOx." target="_blank">Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive
• Hazardous Substances Data: 5776-49-8(Hazardous Substances Data)

Usage

General Description

Phosphoramide mustard cyclohexamine salt is a chemical compound that is derived from nitrogen mustard, a type of chemical warfare agent that was first used during World War I. It is a highly toxic, alkylating agent that is known for its ability to damage DNA and interfere with the cell division process. Phosphoramide mustard cyclohexamine salt has also been studied for its potential use in cancer treatment, particularly in the treatment of certain types of leukemia and lymphoma. However, its use is limited due to its high toxicity and potential for serious side effects. Despite this, research into the potential therapeutic applications of this compound continues, as scientists seek to better understand its mechanisms of action and explore ways to minimize its toxic effects while harnessing its anti-cancer properties.