600-29-3 Usage
Uses
Used in Organic Synthesis:
1H-Pyrrole, 1,2-dimethylserves as a key intermediate in organic synthesis, facilitating the creation of a wide range of chemical compounds.
Used in Pharmaceutical Production:
As an intermediate, 1H-Pyrrole, 1,2-dimethylis instrumental in the production of various pharmaceuticals, contributing to the development of new medications and therapies.
Used in Agrochemicals:
1H-Pyrrole, 1,2-dimethylalso plays a role in the agrochemical industry, where it is used in the synthesis of substances designed to enhance crop protection and yield.
Used in Material Science:
1H-Pyrrole, 1,2-dimethylis utilized in material science, particularly for the development of polymers and organic electronics, due to its unique chemical properties.
Used in Research and Development:
The potential biological activities of 1H-Pyrrole, 1,2-dimethylare under investigation, with research being conducted to explore its pharmacological properties and possible applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 600-29-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 600-29:
(5*6)+(4*0)+(3*0)+(2*2)+(1*9)=43
43 % 10 = 3
So 600-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N/c1-6-4-3-5-7(6)2/h3-5H,1-2H3
600-29-3Relevant academic research and scientific papers
Thermolysis of Polyazapentadienes. Part 8. The formation of Pyrroles from 1,1-Dialkyl-5-aryl-1,5-diazapentadienes
McNab, Hamish,Murray, M. Elizabeth-Ann
, p. 333 - 338 (2007/10/02)
Flash vacuum pyrolysis of the 1,5-diazapentadienes (4)-(10) gave moderate yields of pyrroles together with quinolines, formed by electrocyclic ring closure with elimination.The pyrroles were formed by hydrogen transfer from an N-alkyl group, followed by cyclisation and final aromatisation of the resulting dihydropyrrole intermediate by free-radical cleavage.The mechanism of the hydrogen transfer and cyclisation is not known with certainty, but may involve diradicals or 1,5-dipolar intermediates.
