30186-45-9 Usage
Uses
Used in the Fragrance Industry:
1-isopropyl-1H-pyrrole-3-carbaldehyde(SALTDATA: FREE) is used as a perfume ingredient for its characteristic and appealing odor, contributing to the creation of various fragrances in perfumes, cosmetics, and other scented products.
Used in Pharmaceutical and Fine Chemical Synthesis:
As a key intermediate in organic synthesis, 1-isopropyl-1H-pyrrole-3-carbaldehyde(SALTDATA: FREE) is used as a building block in the production of pharmaceuticals and fine chemicals, facilitating the development of new compounds with therapeutic and industrial applications.
Used in the Development of New Materials:
1-isopropyl-1H-pyrrole-3-carbaldehyde(SALTDATA: FREE) is utilized in the research and development of innovative materials, potentially leading to advancements in various industries that benefit from novel material properties.
Used as a Reagent in Chemical Research and Development:
In the realm of chemical research, 1-isopropyl-1H-pyrrole-3-carbaldehyde(SALTDATA: FREE) serves as a reagent, enabling scientists to explore new chemical reactions and mechanisms, thus expanding the understanding of organic chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 30186-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,8 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30186-45:
(7*3)+(6*0)+(5*1)+(4*8)+(3*6)+(2*4)+(1*5)=89
89 % 10 = 9
So 30186-45-9 is a valid CAS Registry Number.
30186-45-9Relevant academic research and scientific papers
Direct and efficient synthesis of pyrrole-3-carbaldehydes by Vilsmeier-Haack formylation of pyrroles with sterically crowded amides
Ilyin, Petrv.,Pankova, Alenas.,Kuznetsov, Mikhail A.
experimental part, p. 1353 - 1358 (2012/07/03)
A simple and convenient synthetic method to prepare N-substituted pyrrole-3-carbaldehydes by Vilsmeier-Haack formylation of pyrroles using sterically crowded formamides was developed. The dependence of the formylation regioselectivity on steric features of substrates and reagents is discussed. Georg Thieme Verlag Stuttgart · New York.
