199851-22-4 Usage
Uses
Used in Organic Synthesis:
4-CHLORO-2-(TERT-BUTYLAMINO)-5-THIAZOLECARBOXALDEHYDE is utilized as a key intermediate in organic synthesis for the creation of complex organic molecules. Its unique functional groups facilitate multiple reaction pathways, making it a versatile component in the construction of diverse chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-CHLORO-2-(TERT-BUTYLAMINO)-5-THIAZOLECARBOXALDEHYDE serves as a crucial component in drug discovery and development. Its incorporation into the molecular structures of potential drugs can lead to new therapeutic agents with improved efficacy and selectivity.
Used in Drug Development:
4-CHLORO-2-(TERT-BUTYLAMINO)-5-THIAZOLECARBOXALDEHYDE is employed as a building block in the development of new drugs. Its biological activity and pharmacological properties make it a promising candidate for the treatment of various diseases and conditions.
Used in Agrochemical Development:
In the agrochemical sector, 4-CHLORO-2-(TERT-BUTYLAMINO)-5-THIAZOLECARBOXALDEHYDE is used as a starting material for the synthesis of novel agrochemicals. Its potential applications include the development of pesticides, herbicides, and other crop protection agents, contributing to enhanced agricultural productivity and sustainability.
Check Digit Verification of cas no
The CAS Registry Mumber 199851-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,8,5 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 199851-22:
(8*1)+(7*9)+(6*9)+(5*8)+(4*5)+(3*1)+(2*2)+(1*2)=194
194 % 10 = 4
So 199851-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H11ClN2OS/c1-8(2,3)11-7-10-6(9)5(4-12)13-7/h4H,1-3H3,(H,10,11)
199851-22-4Relevant academic research and scientific papers
Improved Synthesis of 2-Substituted 4-Chlorothiazole-5-carbaldehydes
Debski, Norbert,Hanefeld, Wolfgang,Schlitzer, Martin
, p. 1427 - 1429 (2007/10/03)
An improved method for the reaction of 2,4-dichlorothiazole-5-carbaldehyde (2) with secondary amines was established using potassium carbonate in acetonitrile at room temperature instead of deprotonation with butyllithium in tetrahydrofuran at -78°. The m
