35213-85-5

Basic information

• Product Name: 5-METHYLTETRAZOLO[1,5-A]QUINOLINE
• Synonyms: 5-METHYLTETRAZOLO[1,5-A]QUINOLINE;AURORA KA-6570
• CAS NO: 35213-85-5
• Molecular Formula: C10H8N4
• Molecular Weight: 184.2
• Mol File: 35213-85-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.39g/cm³
• Refractive Index: 1.752
• CAS DataBase Reference: 5-METHYLTETRAZOLO[1,5-A]QUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHYLTETRAZOLO[1,5-A]QUINOLINE(35213-85-5)
• EPA Substance Registry System: 5-METHYLTETRAZOLO[1,5-A]QUINOLINE(35213-85-5)

Safety Data

• Hazardous Substances Data: 35213-85-5(Hazardous Substances Data)

Usage

General Description

5-METHYLTETRAZOLO[1,5-A]QUINOLINE is a chemical compound with the molecular formula C11H10N4. It belongs to the tetrazoloquinolines class and is a heterocyclic compound containing both nitrogen and carbon atoms. 5-METHYLTETRAZOLO[1,5-A]QUINOLINE has potential applications as a fluorescent probe for detecting metal ions due to its ability to form complexes with certain metals. It also exhibits antimicrobial and antitumor activities, making it a target for further studies in the fields of medicine and pharmaceuticals. Additionally, it has been investigated for its potential to act as a photosensitizer in photodynamic therapy, a treatment for cancer and other diseases. Overall, 5-METHYLTETRAZOLO[1,5-A]QUINOLINE is a versatile compound with potential applications in various fields including medicine, chemistry, and materials science.

InChI:InChI=1/C10H8N4/c1-7-6-10-11-12-13-14(10)9-5-3-2-4-8(7)9/h2-6H,1H3

Upstream product

• 4437-65-4 4-methyl-2-thioxo-1H-quinoline 
• 21703-52-6 2-hydrazinyl-4-methylquinoline 
• 634-47-9 2-chloro-4-methylquinoline 

Downstream Products

• 1224886-25-2 C₁₈H₁₈N₄ 
• 1224886-26-3 C₁₉H₁₆N₄ 
• 1224886-24-1 4-methyl-2-(4-phenyl-1H-1,2,3-triazol-1-yl)quinoline 

Relevant articles and documents

Efficient uncatalyzed conversion of primary and secondary thioamides into 1-substituted, 5-substituted, 1, 5-disubstituted and annulated tetrazoles

Unprecedented high-yield simple and mild conversion of primary aliphatic and aromatic thioamides into 5-substituted tetrazoles on treatment with a combination of tetrachlorosilane and sodium azide in refluxing acetonitrile has been achieved. Secondary acyclic, cyclic, and heterocyclic thioamides could also be transformed in high yields into 1-substituted, 1,5-disubstituted, or annulated tetrazoles under the same reaction condition. Copyright Taylor & Francis Group, LLC.

Microwave assisted synthesis and antifungal activity of 1,2,4-triazine, 1,2,4-triazole, tetrazole and pyrazole derivatives

The condensation reactions of 2-hydrazino-4-methylquinoline with diethyl oxalate, ethyl bromoacetate, aromatic aldehydes, acetic anhydride, nitrous acid and different acetophenones followed by DMF and POCl3 under microwave irradiation and by conventional methods are described. The reaction rate is enhanced tremendously under microwave irradiation as compared to conventional method with improved yields. All the newly synthesised compounds have been screened for antifungal activity against fungi A. niger andA.flavous.