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(tert-butyl)quinoline


  • CasNo 61702-91-8
  • Purity 99%
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What is the (tert-butyl)quinoline ?

(tert-butyl)quinoline is , while it's Molecular Formula is C13H15N. Used in Pharmaceutical Industry:
(tert-butyl)quinoline is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical structure and biological activities, which include anti-inflammatory, antibacterial, antifungal, and antioxidant properties. These properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (tert-butyl)quinoline is utilized as a key component in the synthesis of various agrochemicals. Its biological activities, such as antibacterial and antifungal properties, contribute to the development of effective compounds for crop protection and disease management.
Used in Organic Chemistry:
(tert-butyl)quinoline serves as an important intermediate in organic chemistry for the synthesis of a wide range of organic compounds. Its unique structure allows for various chemical reactions, making it a valuable tool for the creation of complex organic molecules.
Used in Drug Development:
(tert-butyl)quinoline is employed in drug development as a potential precursor for new therapeutic agents. Its biological activities and chemical properties are being studied to explore its potential in treating various diseases and conditions, enhancing its applicability in the pharmaceutical field.

What is the CAS number for (tert-butyl)quinoline ?

The CAS number of (tert-butyl)quinoline is 61702-91-8.

More information of (tert-butyl)quinoline 61702-91-8 are:

CAS?Number

61702-91-8

Molecular Formula

C13H15N

Molecular Weight

185.2649

Density

1.009g/cm3

Boiling Point

286.2°Cat760mmHg

Flash Point

116.3°C

What is (tert-butyl)quinoline (61702-91-8) used for?

(tert-butyl)quinoline, also known as 2-(tert-butyl)quinoline, is a chemical compound characterized by the molecular formula C13H17N. It is a substituted quinoline derivative distinguished by the attachment of a tert-butyl group to the nitrogen atom. (tert-butyl)quinoline is recognized for its diverse biological activities, such as anti-inflammatory, antibacterial, antifungal, and antioxidant properties, and is a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its potential in the development of new drugs and therapeutic agents is currently under investigation.

InChI:InChI=1/C13H15N/c1-13(2,3)12-9-8-10-6-4-5-7-11(10)14-12/h4-9H,1-3H3

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