499771-03-8

Basic information

• Product Name: 1,3,4-THIADIAZOL-2-YLMETHANOL,97%
• Synonyms: 1,3,4-THIADIAZOL-2-YLMETHANOL,97%;1,3,4-Thiadiazol-2-ylmethanol
• CAS NO: 499771-03-8
• Molecular Formula: C₃H₄N₂OS
• Molecular Weight: 116.14166
• Mol File: 499771-03-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3,4-THIADIAZOL-2-YLMETHANOL,97%(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4-THIADIAZOL-2-YLMETHANOL,97%(499771-03-8)
• EPA Substance Registry System: 1,3,4-THIADIAZOL-2-YLMETHANOL,97%(499771-03-8)

Safety Data

• Safety Statements: S24/25:Avoid contact with skin and eyes.
• Hazardous Substances Data: 499771-03-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1,3,4-Thiadiazol-2-ylmethanol, 97% is used as an intermediate in the synthesis of pharmaceutical drugs for its unique structural properties and reactivity. It plays a crucial role in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
1,3,4-Thiadiazol-2-ylmethanol, 97% is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Organic Synthesis:
1,3,4-Thiadiazol-2-ylmethanol, 97% serves as a key building block in organic synthesis, enabling the production of a wide range of pharmaceuticals and agrochemicals. Its high purity level of 97% ensures precise and consistent chemical composition, making it suitable for use in research, development, and manufacturing processes.

Upstream product

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Relevant articles and documents

Azo dyes containing 1,3,4-thiadiazole fragment: Synthesis and properties

New 1,3,4-thiadiazole derivatives containing a diazenyl group, as well as both a diazenyl and an imino group, were synthesized and their optical and thermal properties were investigated. Initially, new azo compounds containing an azo group directly in the thiadiazole block were obtained by the coupling of diazonium bisulfates based on the previously known 5-derivatives of 2-amino-1,3,4-thiadiazoles with N,N-dialkyl anilines (N(n-Bu)2, NEt2, and NEt(EtOH)). Schiff bases were obtained by the interaction of p-toluidine, p-phenylenediamine and p-aminophenol with azo compounds containing an aldehyde group in the 1,3,4-thiadiazole ring. The new dyes were characterized by spectral (IR, UV, 1H NMR, 13C NMR and mass spectra) and X-ray analyses. This journal is

CARBACEPHEM BETA-LACTAM ANTIBIOTICS

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