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36647-76-4

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36647-76-4 Usage

General Description

2,2-dioxido-6,12-dioxo-3-oxa-2lambda~6~-thia-7,11-diazatetradecan-14-yl methanesulfonate is a complex chemical compound that is used in pharmaceuticals and chemical research. Its molecular structure consists of a long chain of carbon and nitrogen atoms, with multiple oxygen and sulfur atoms as part of the functional groups. The presence of the methanesulfonate group suggests that it may be used as a protecting group in organic synthesis. The compound's intricate structure and functional groups make it a versatile molecule with potential applications in medicinal chemistry and other scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 36647-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,4 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36647-76:
(7*3)+(6*6)+(5*6)+(4*4)+(3*7)+(2*7)+(1*6)=144
144 % 10 = 4
So 36647-76-4 is a valid CAS Registry Number.

36647-76-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[3-(3-methylsulfonyloxypropanoylamino)propylamino]-3-oxopropyl]

1.2 Other means of identification

Product number -
Other names 1.3-Bis-(3-methan sulfonyloxy-propionylamino)-propan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36647-76-4 SDS

36647-76-4Downstream Products

36647-76-4Relevant articles and documents

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

Senning,Buchholt,Bierling

, p. 1800 - 1809 (2007/10/05)

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.

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