912669-58-0

Basic information

• Product Name: 1,3,4-Thiadiazole-2-methanol, 5-chloro-
• Synonyms: 1,3,4-Thiadiazole-2-methanol, 5-chloro-;(5-chloro-1,3,4-thiadiazol-2-yl)methanol;5-Chloro-1,3,4-thiadiazole-2-methanol
• CAS NO: 912669-58-0
• Molecular Formula: C3H3ClN2OS
• Molecular Weight: 150.59
• Mol File: 912669-58-0.mol

Chemical Properties

• Boiling Point: 309.968°C at 760 mmHg
• Flash Point: 141.264°C
• Appearance: /
• Density: 1.653g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.624
• Storage Temp.: 2-8°C
• PKA: 12.20±0.10(Predicted)
• CAS DataBase Reference: 1,3,4-Thiadiazole-2-methanol, 5-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4-Thiadiazole-2-methanol, 5-chloro-(912669-58-0)
• EPA Substance Registry System: 1,3,4-Thiadiazole-2-methanol, 5-chloro-(912669-58-0)

Safety Data

• Hazardous Substances Data: 912669-58-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1,3,4-Thiadiazole-2-methanol, 5-chlorois used as a building block for the synthesis of biologically active molecules, contributing to the development of new pharmaceutical compounds. Its unique structure allows for the creation of diverse molecules with potential therapeutic properties.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1,3,4-Thiadiazole-2-methanol, 5-chlorois utilized as a building block for the synthesis of active ingredients in fungicides and herbicides. Its chemical properties make it a promising candidate for the development of effective crop protection agents.
Used in Research and Development:
1,3,4-Thiadiazole-2-methanol, 5-chlorois also used in research and development settings to explore its chemical properties and potential applications. Its unique structure and reactivity make it an interesting molecule for further study, potentially leading to new discoveries and applications in various fields.

InChI:InChI=1/C3H3ClN2OS/c4-3-6-5-2(1-7)8-3/h7H,1H2

Upstream product

• 64837-49-6 5-chloro-1,3,4-thiadiazole-2-carboxylic acid ethyl ester 

Relevant articles and documents

Aryl hetero ring-substituted aromatic compound (by machine translation)

[Problem] β - lactamase inhibiting action in a new compound. (1A) or (1b) or a compound represented by the formula [a] to pharmaceutically acceptable salts. [(1A) (1b) and in the formula, g is, O, etc. S; X is, a hydroxyl group, an alkoxy group such as C1

USE OF SPIRO-OXINDOLE COMPOUNDS AS THERAPEUTIC AGENTS

This invention is directed to methods of using spiro-oxindole compounds of formula (I): wherein k, j, Q, R1, R2a, R2b, R2c, R2d, R3a, R3b, R3c, and R3d are as defined herein, as a stereoisomer, enantiomer, tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt, solvate or prodrug thereof, for the treatment and/or prevention of hypercholesterolemia, benign prostatic hyperplasia, pruritis and cancer.

SPIRO-OXINDOLE COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS

This invention is directed to spiro-oxindole compounds of formula (I): wherein k, j, Q, R1, R2a, R2b, R2c, R2d, R3a, R3b, R3c, and R3d are as defined herein, as a stereoisomer, enantiomer, tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt, solvate or prodrug thereof, which are useful for the treatment and/or prevention of sodium channel-mediated diseases or conditions, such as pain. Pharmaceutical compositions comprising the compounds and methods of preparing and using the compounds are also disclosed.