29212-49-5 Usage
General Description
1H-Pyrrol-3-amine(9CI) is a chemical compound known for its role in organic chemistry. It is categorized as an amine, which are organic compounds that contain a basic nitrogen atom with a lone pair, and a heterocyclic compound, which are organic compounds that contain atoms of at least two different elements as members of its rings. Its structure consists of a pyrrole ring, a five-membered aromatic ring with one nitrogen atom, and a functional amino group (NH2). 1H-Pyrrol-3-amine(9CI) is often used in chemical synthesis, particularly in the production of various pharmaceuticals and complex organic molecules due to its reactivity and versatility. It commonly appears as a colorless or pale yellow liquid and should be handled with care due to its potential health and environmental hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 29212-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29212-49:
(7*2)+(6*9)+(5*2)+(4*1)+(3*2)+(2*4)+(1*9)=105
105 % 10 = 5
So 29212-49-5 is a valid CAS Registry Number.
29212-49-5Relevant articles and documents
3-aminopyrroles, methods for their synthesis and for their pharmaceutical use
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, (2008/06/13)
The invention is directed to 3-aminopyrroles of formula I, which are largely new, to methods for the preparation and to their use as medicinal agents and preparations, as well as to anti-convulsive or analgesic preparations containing these 3-aminopyrroles. Disubstituted and monosubstituted amino groups are claimed as 3-amino substituents. The invention pursues the objective of developing largely new 3-aminopyrroles, which have CNS activity, particularly ones which anti-convulsive or analgesic properties, as well as methods for their preparation and their use as medicinal preparations. Pursuant to the invention, the synthesis is carried out by cyclizing open-chain precursors, such as aminoacrylic acid derivative, or by modifying pyrroles.
