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281193-14-4

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  • 1,4,7,10-TETRA-N-(DIETHYLPHOSPHONOAZA)DECANE

    Cas No: 281193-14-4

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281193-14-4 Usage

Type of compound

Phosphorus-containing compound

Structure

Long hydrocarbon chain and an amine group

Nature

Amphiphilic

Potential applications

Drug delivery, catalysis, surfactant

Biological properties

Antibacterial and antifungal properties

Industrial applications

Various, due to its unique structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 281193-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,1,1,9 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 281193-14:
(8*2)+(7*8)+(6*1)+(5*1)+(4*9)+(3*3)+(2*1)+(1*4)=134
134 % 10 = 4
So 281193-14-4 is a valid CAS Registry Number.

281193-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,7,10-TETRA-N-(DIETHYLPHOSPHONOAZA)DECANE

1.2 Other means of identification

Product number -
Other names 1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetraacetamide

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:281193-14-4 SDS

281193-14-4Downstream Products

281193-14-4Relevant articles and documents

Synthesis of an azacrown template for phosphatidylinositol-4,5-bis(phosphate) recognition

Gray Jr., Charles W.,Barry, Kathleen,Lindberg, Eric J.,Houston, Todd A.

, p. 2683 - 2686 (2007)

An azacrown system has been developed for selective membrane binding of phosphatidylinositol-4,5-bis(phosphate) recognition. Neutral and cationic forms of the metacyclophane macrocycles have been synthesized by divergent routes in acceptable yields. Such

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