30186-46-0 Usage
Uses
Used in Pharmaceutical Industry:
1-TERT-BUTYL-1H-PYRROLE-3-CARBALDEHYDE serves as an intermediate in the synthesis of various pharmaceuticals, playing a crucial role in the development of new drugs and medicinal compounds.
Used in Fragrance and Flavor Industry:
1-TERT-BUTYL-1H-PYRROLE-3-CARBALDEHYDE is utilized in the production of fragrances and flavors, where its unique properties contribute to the creation of distinct scents and tastes.
Used in Specialty Chemicals Production:
1-TERT-BUTYL-1H-PYRROLE-3-CARBALDEHYDE is employed in the synthesis of specialty chemicals, which are used across a wide range of industries for their specific properties and applications.
Overall, 1-TERT-BUTYL-1H-PYRROLE-3-CARBALDEHYDE is a multifaceted chemical compound with applications in various industries, including pharmaceuticals, fragrances and flavors, and specialty chemicals production, due to its stability and suitability in chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 30186-46-0 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 30186-46:
(7*3)+(6*0)+(5*1)+(4*8)+(3*6)+(2*4)+(1*6)=90
90 % 10 = 0
So 30186-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-9(2,3)10-5-4-8(6-10)7-11/h4-7H,1-3H3
30186-46-0Relevant academic research and scientific papers
COMPOUNDS AND USES THEREOF
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Page/Page column 139, (2020/08/22)
The present disclosure features compounds useful for the treatment of BAF complex-related disorders.
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.
3-formylpyrroles from 3-furfurylamines by bromine oxidation reaction
Harn, Piin-Jye,Lin, Chu-Chung,Wu, Hsien-Jen
experimental part, p. 1321 - 1326 (2011/10/07)
Oxidation of 3-furfurylamines 3a-e with bromine in acetone-water solution gave N-substituted 3-formylpyrroles 4a-e in good yields. A reaction mechanism via the Clauson-Kaas reaction followed by the cis-trans isomerization of the 2-ene-1,4-diones 13 and 14
