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Pyrrolidine, 1-[(4-fluorophenyl)azo]is a chemical compound with the molecular formula C10H12FN3. It is characterized by its azo group, which is a functional group comprised of two nitrogen atoms linked by a double bond, and a pyrrolidine ring, which is a five-membered heterocyclic ring containing four carbon atoms and one nitrogen atom. Pyrrolidine, 1-[(4-fluorophenyl)azo]is commonly used as a dye intermediate in the production of colorants and pigments.

96783-59-4

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96783-59-4 Usage

Uses

Used in Textile Industry:
Pyrrolidine, 1-[(4-fluorophenyl)azo]is used as a dye intermediate for imparting color to fabrics and textiles. Its ability to produce a wide range of colors makes it a valuable component in the textile industry.
Used in Printing Industry:
In the printing industry, Pyrrolidine, 1-[(4-fluorophenyl)azo]is used as a dye intermediate to create colorants for ink production. This allows for the creation of vibrant and long-lasting prints on various materials.
Used in Cosmetics Industry:
Pyrrolidine, 1-[(4-fluorophenyl)azo]is used as a dye intermediate in the cosmetics industry to add color to various products such as makeup, hair dyes, and nail polishes. Its versatility in color production makes it a popular choice for these applications.
Potential Use in Pharmaceutical and Medicinal Chemistry:
Due to its structural properties, Pyrrolidine, 1-[(4-fluorophenyl)azo]may have potential uses in pharmaceuticals and medicinal chemistry. However, further research and development would be required to explore and confirm its applications in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 96783-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,8 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96783-59:
(7*9)+(6*6)+(5*7)+(4*8)+(3*3)+(2*5)+(1*9)=194
194 % 10 = 4
So 96783-59-4 is a valid CAS Registry Number.

96783-59-4SDS

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-fluorophenyl)-2-(pyrrolidin-1-yl)diazene

1.2 Other means of identification

Product number -
Other names 1-((4-fluorophenyl)diazenyl)pyrrolidine

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:96783-59-4 SDS

96783-59-4Relevant academic research and scientific papers

Synthesis of triazenes with nitrous oxide

Kiefer, Gregor,Riedel, Tina,Dyson, Paul J.,Scopelliti, Rosario,Severin, Kay

, p. 302 - 305 (2015)

Triazenes are valuable compounds in organic chemistry and numerous applications have been reported. Furthermore, triazenes have been investigated extensively as potential antitumor drugs. Here, we describe a new method for the synthesis of triazenes. The procedure involves a reagent which is rarely used in synthetic organic chemistry: nitrous oxide (N2O, laughing gas ). Nitrous oxide mediates the coupling of lithium amides and organomagnesium compounds while serving as a nitrogen donor. Despite the very inert character of nitrous oxide, the reactions can be performed in solution under mild conditions. A key advantage of the new procedure is the ability to access triazenes with alkynyl and alkenyl substituents. These compounds are difficult to prepare by conventional methods because the required starting materials are unstable. Some of the new alkynyltriazenes were found to display high cytotoxicity in in vitro tests on ovarian and breast cancer cell lines.

PREPARATION AND MEDICAL USE OF TRIAZENES

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Page/Page column 23; 24; 27; 28, (2016/01/25)

The present invention relates to a novel method for preparing triazenes. Further, the invention relates to novel triazenes and the use of N2O for preparing a compound comprising a triazene group. Further, the invention relates to the use of the

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