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2-methyl-N-[6-[(2-methylaziridine-1-carbonyl)amino]hexyl]aziridine-1-carboxamide is a heterocyclic organic compound belonging to the aziridine family, characterized by its unique structure featuring two aziridine rings connected by a hexyl chain. 2-methyl-N-[6-[(2-methylaziridine-1-carbonyl)amino]hexyl]aziridine-1-carboxamide, with the molecular formula C15H28N4O2, is distinguished by the presence of a carbonyl group and an amine group attached to the first aziridine ring, endowing it with versatile chemical and pharmaceutical properties.

3901-51-7

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3901-51-7 Usage

Uses

Used in Pharmaceutical Applications:
2-methyl-N-[6-[(2-methylaziridine-1-carbonyl)amino]hexyl]aziridine-1-carboxamide is utilized as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. Its ability to form stable covalent bonds with biological targets makes it a promising candidate for the development of new drugs with specific therapeutic actions.
Used in Chemical Synthesis:
In the chemical industry, 2-methyl-N-[6-[(2-methylaziridine-1-carbonyl)amino]hexyl]aziridine-1-carboxamide serves as a versatile building block for the creation of complex organic molecules. Its presence of reactive functional groups, such as the carbonyl and amine groups, allows for a wide range of chemical reactions, facilitating the synthesis of novel materials with diverse applications.
Used in Research and Development:
2-methyl-N-[6-[(2-methylaziridine-1-carbonyl)amino]hexyl]aziridine-1-carboxamide is employed as a valuable research tool in the exploration of new chemical reactions and mechanisms. Its unique structure provides insights into the reactivity and selectivity of aziridine compounds, contributing to the advancement of organic chemistry and the discovery of innovative synthetic methods.
Used in Material Science:
In the field of material science, 2-methyl-N-[6-[(2-methylaziridine-1-carbonyl)amino]hexyl]aziridine-1-carboxamide is utilized in the development of new materials with specific properties. Its ability to form stable covalent bonds and its compatibility with various polymers make it a suitable candidate for the creation of high-performance materials with applications in various industries, such as electronics, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 3901-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3901-51:
(6*3)+(5*9)+(4*0)+(3*1)+(2*5)+(1*1)=77
77 % 10 = 7
So 3901-51-7 is a valid CAS Registry Number.

3901-51-7SDS

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 2-methyl-N-[6-[(2-methylaziridine-1-carbonyl)amino]hexyl]aziridine-1-carboxamide

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:3901-51-7 SDS

3901-51-7Downstream Products

3901-51-7Relevant academic research and scientific papers

AZIRIDINE CROSSLINKING AGENTS FOR ACRYLIC ADHESIVES

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, (2010/09/17)

A crosslinkable, pre-adhesive composition is described comprising an acid-functional (meth)acrylate copolymer and an aziridine crosslinking agent, which when crosslinked provides a pressure-sensitive adhesive and pressure-sensitive adhesive articles.

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