36647-85-5

Basic information

• Product Name: 2,2-dioxido-6,15-dioxo-3-oxa-2lambda~6~-thia-7,14-diazaheptadecan-17-yl methanesulfonate
• CAS NO: 36647-85-5
• Molecular Formula: C₁₄H₂₈N₂O₈S₂
• Molecular Weight: 416.5107
• Mol File: 36647-85-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 771.9°C at 760 mmHg
• Flash Point: 420.6°C
• Density: 1.276g/cm³
• Vapor Pressure: 9.48E-24mmHg at 25°C
• Refractive Index: 1.497
• CAS DataBase Reference: 2,2-dioxido-6,15-dioxo-3-oxa-2lambda~6~-thia-7,14-diazaheptadecan-17-yl methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dioxido-6,15-dioxo-3-oxa-2lambda~6~-thia-7,14-diazaheptadecan-17-yl methanesulfonate(36647-85-5)
• EPA Substance Registry System: 2,2-dioxido-6,15-dioxo-3-oxa-2lambda~6~-thia-7,14-diazaheptadecan-17-yl methanesulfonate(36647-85-5)

Safety Data

• Hazardous Substances Data: 36647-85-5(Hazardous Substances Data)

Usage

General Description

2,2-dioxido-6,15-dioxo-3-oxa-2lambda~6~-thia-7,14-diazaheptadecan-17-yl methanesulfonate is a chemical compound that belongs to the class of sulfonate esters. It is a synthetic organic compound with a complex structure that contains multiple oxygen, sulfur, nitrogen, and carbon atoms. The presence of the methanesulfonate group indicates that it is a derivative of methanesulfonic acid. 2,2-dioxido-6,15-dioxo-3-oxa-2lambda~6~-thia-7,14-diazaheptadecan-17-yl methanesulfonate may have potential applications in various fields including pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties. It is likely to have specific functions or reactivity related to its molecular structure, and further research and analysis would be required to fully understand its potential uses and implications.

Upstream product

• 36648-02-9 3-Iodo-N-[6-(3-iodo-propionylamino)-hexyl]-propionamide 
• 2386-52-9 silver methanesulfonate 

Relevant articles and documents

Novel Bis-sulfonic Acid Esters with Cytostatic Activity (author's transl)

The introduction of electron-withdrawing groups into the group R of piposulfan analogs R--SO2--O--X--O--SO2--R substantially increases their antileukemic activity in animal tests (leukemia L 1210). The central moiety X can be varied considerably (provided it contains amide groups) without appreciable loss of activity. A number of busulfan analogs as well as busulfan itself proved to be practically inactive against murine leukemia L 1210. Among a total of 122 bis-sulfonic acid esters tested 35 gave a survival time index of 150% or more after i.p. application and 5 after oral application.