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2,2-bis(butylsulfonyl)-N,N-bis(4-methoxyphenyl)ethene-1,1-diamine is a complex organic chemical compound characterized by its ethene backbone to which two butylsulfonyl groups and two methoxyphenyl groups are attached. This diamine compound is known for its unique chemical structure and reactivity, making it a valuable reagent in organic synthesis and chemical research.

5161-03-5

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5161-03-5 Usage

Uses

Used in Organic Synthesis:
2,2-bis(butylsulfonyl)-N,N-bis(4-methoxyphenyl)ethene-1,1-diamine is used as a reagent for the synthesis of various organic molecules. Its unique structure allows it to participate in a range of chemical reactions, facilitating the creation of new compounds with potential applications across different industries.
Used in Chemical Research:
In the field of chemical research, 2,2-bis(butylsulfonyl)-N,N-bis(4-methoxyphenyl)ethene-1,1-diamine serves as a catalyst or building block, contributing to the advancement of chemical knowledge and the development of novel materials and compounds.
Used in Pharmaceutical Industry:
2,2-bis(butylsulfonyl)-N,N-bis(4-methoxyphenyl)ethene-1,1-diamine is used as an intermediate or catalyst in the production of pharmaceuticals. Its unique chemical properties may contribute to the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
2,2-bis(butylsulfonyl)-N,N-bis(4-methoxyphenyl)ethene-1,1-diamine is also utilized in the agrochemical sector, where it may be employed in the synthesis of pesticides, herbicides, or other agricultural chemicals. Its reactivity and structural features can be harnessed to create more effective and environmentally friendly products.
Used in Materials Science:
2,2-bis(butylsulfonyl)-N,N-bis(4-methoxyphenyl)ethene-1,1-diamine has potential applications in materials science, where it could be used to develop new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
It is crucial to handle 2,2-bis(butylsulfonyl)-N,N-bis(4-methoxyphenyl)ethene-1,1-diamine with care due to its potential hazards if not properly managed or used. Safety precautions should be observed to ensure the well-being of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 5161-03-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,6 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5161-03:
(6*5)+(5*1)+(4*6)+(3*1)+(2*0)+(1*3)=65
65 % 10 = 5
So 5161-03-5 is a valid CAS Registry Number.

5161-03-5SDS

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 2,2-bis(butylsulfonyl)-1-N,1-N'-bis(4-methoxyphenyl)ethene-1,1-diamine

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

More Details:5161-03-5 SDS

5161-03-5Upstream product

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