1258934-68-7

Basic information

• Product Name: tert-Butyl (5-iodothiazol-4-yl)carbaMate
• Synonyms: tert-Butyl (5-iodothiazol-4-yl)carbaMate
• CAS NO: 1258934-68-7
• Molecular Formula: C₈H₁₁IN₂O₂S
• Molecular Weight: 326.15461
• Mol File: 1258934-68-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: tert-Butyl (5-iodothiazol-4-yl)carbaMate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-Butyl (5-iodothiazol-4-yl)carbaMate(1258934-68-7)
• EPA Substance Registry System: tert-Butyl (5-iodothiazol-4-yl)carbaMate(1258934-68-7)

Safety Data

• Hazardous Substances Data: 1258934-68-7(Hazardous Substances Data)

Usage

General Description

Tert-butyl (5-iodothiazol-4-yl)carbamate is a chemical compound that belongs to the family of carbamate derivatives. It is a white to off-white solid with a molecular formula of C9H12IN2O2S and a molecular weight of 340.17 g/mol. tert-Butyl (5-iodothiazol-4-yl)carbaMate is commonly used in organic synthesis as a reagent for the synthesis of various functionalized molecules. It is stable under normal conditions of use and storage, and should be handled with care due to its potential for irritation and toxicity. Tert-butyl (5-iodothiazol-4-yl)carbamate has potential applications in the pharmaceutical and agrochemical industries due to its unique structure and properties.

Upstream product

• 1235406-42-4 thiazol-4-ylaminocarboxylic acid tert-butyl ester 

Downstream Products

• 1258934-71-2 tert-butyl N-{5-[2-(4-fluorophenyl)ethynyl]-1,3-thiazol-4-yl}carbamate 
• 1235406-42-4 thiazol-4-ylaminocarboxylic acid tert-butyl ester 
• 1258934-72-3 C₁₁H₇FN₂S 
• 1258934-78-9 tert-butyl N-(5-{3-[(benzylamino)phenyl]ethynyl}-1,3-thiazol-4-yl)carbamate 
• 1258934-97-2 tert-butyl N-[5-(3-phenylprop-1-ynyl)-1,3-thiazol-4-yl]carbamate 
• 1258934-77-8 tert-butyl N-{5-[(3-hydroxyphenyl)ethynyl]-1,3-thiazol-4-yl}carbamate 
• 1258934-75-6 tert-butyl N-{5-[(3-aminophenyl)ethynyl]-1,3-thiazol-4-yl}carbamate 
• 1258934-82-5 tert-butyl N-{2-(2-aminopyrimidin-5-yl)-5-[2-(4-fluorophenyl)ethynyl]-1,3-thiazol-4-yl}carbamate 
• 1258934-81-4 tert-butyl N-{2-chloro-5-[2-(4-fluorophenyl)ethynyl]-1,3-thiazol-4-yl}carbamate 
• 1258934-95-0 6-benzyl-4H-pyrrolo[2,3-d]thiazole 

Relevant articles and documents

TRICYCLIC COMPOUNDS AS GLYCOGEN SYNTHASE KINASE 3 (GSK3) INHIBITORS AND USES THEREOF

The present disclosure provides compounds of Formula (I), and salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, isotopically labeled derivatives, and prodrugs thereof. The provided compounds may be useful for inhibiting kinases

HETEROARYL COMPOUNDS AS AGROCHEMICAL FUNGICIDES

Heteroaryl compounds as agrochemical fungicides Formula (I) The present invention relates to heteroaryl compounds of formula (I) or a compound in the form of a stereoisomer, an agriculturally acceptable salt, a tautomer, an isotopic form, a N-oxide, a S- oxide, a prodrug or mixture thereof. The present invention further relates to the use of a com- pound of formula (I). Furthermore, the present invention relates to methods for combating phy- topathogenic harmful fungi, which methods comprising the steps of treatment of the phytopatho- genic fungi, the plant orthe plant propagation material selected from seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, including seedlings and young plants to be protected against fungal attack, stored materials or harvest, or alternatelythe locus or soil or soil substituents or surfaces therefrom, with at least one compound of formula (I).

Novel syntheses of variably substituted pyrrolo[2,3-d]thiazoles

Pyrrolo[2,3-d]thiazoles are conveniently derived from the corresponding o-aminoalkynylthiazoles via microwave assisted 5-endo-dig cyclization. Methylene-bridged substituents in the 6-position are directly obtained from 5-exo-Heck cyclization based on the