60024-89-7 Usage
Uses
Used in Pharmaceutical Industry:
Tert-butyl 4-(3-methoxy-3-oxopropyl)-3,5-dimethyl-1H-pyrrole-2-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals. Its versatile reactivity and functional group tolerance make it suitable for the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, tert-butyl 4-(3-methoxy-3-oxopropyl)-3,5-dimethyl-1H-pyrrole-2-carboxylate is utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure and properties contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Organic Synthesis:
Tert-butyl 4-(3-methoxy-3-oxopropyl)-3,5-dimethyl-1H-pyrrole-2-carboxylate is employed as a versatile building block in organic synthesis for the production of complex organic compounds. Its unique structure and properties enable the synthesis of a wide range of organic compounds with diverse applications in various industries.
Used in Medicinal Chemistry:
In medicinal chemistry, tert-butyl 4-(3-methoxy-3-oxopropyl)-3,5-dimethyl-1H-pyrrole-2-carboxylate is used as a valuable tool for the development of new therapeutic agents. Its unique structure and properties allow for the design and synthesis of novel compounds with potential therapeutic applications in various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 60024-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60024-89:
(7*6)+(6*0)+(5*0)+(4*2)+(3*4)+(2*8)+(1*9)=87
87 % 10 = 7
So 60024-89-7 is a valid CAS Registry Number.
60024-89-7Relevant academic research and scientific papers
Synthesis of orthogonally protected pyrrole tricarboxylic acid derivatives: Versatile building blocks for pyrrole-containing compounds
Schmuck, Carsten,Rupprecht, Daniel,Urban, Christian,Walden, Nicholas
, p. 89 - 96 (2007/10/03)
The large-scale synthesis of three new orthogonally protected pyrrole tricarboxylates 1-3 is described. Using different cleavage conditions, each of the three carboxylates can be set free selectively without affecting the others, making these pyrrole derivatives versatile synthetic building blocks for a wide range of applications in natural product or supramolecular chemistry. Georg Thieme Verlag Stuttgart.
New Efficient Total Syntheses of Derivatives of Protoporphyrin-IX Bearing Deuterated Methyl Groups
Smith, Kevin M.,Pandey, Ravindra K.
, p. 1383 - 1388 (2007/10/02)
New total syntheses of hemins which are regioselectively deuterated in the 1,5 (2), 5 (3) or 8 (4) methyl groups are described.Syntheses of hemins 2 and 3 follow the progression from pyrromethane 12 to t-butyl tripyrrene-carboxylate hydrobromide (17 and 30) and then to a,c-biladiene dihydrobromide (19 and 31), but for reasons of economy in use of labeled monopyrroles, the a,c-biladiene dihydrobromide 40 for hemin 4 is approached in an initially "clockwise" manner by synthesis of a benzyl tripyrrene-carboxylate hydrobromide 37 from the pyrromethane 5.Cyclization of the a,c-biladienes (19, 31, and 40) was accomplished by brief heating in dimethylformamide in the presence of copper(II) chloride.
