1311314-54-1 Usage
Explanation
Different sources of media describe the Explanation of 1311314-54-1 differently. You can refer to the following data:
1. The compound consists of 8 carbon atoms, 9 hydrogen atoms, 1 nitrogen atom, and 1 oxygen atom.
2. It contains a ring structure with both carbon and a heteroatom (nitrogen) atoms.
3. The compound has a fused pyrrole and pyridine ring system, which contributes to its unique properties.
4. The compound forms a powdery solid with a white to off-white color.
5. The compound dissolves easily in organic solvents but does not dissolve in water.
6. It is used in the study of neurotransmitters and their receptors, which can help in understanding neurological disorders and developing potential treatments.
7. The unique structure and properties of the compound make it a valuable tool in the research of neurological conditions and the development of new therapies.
Type of compound
Heterocyclic compound
Structure
Pyrrolopyridine skeleton
Physical appearance
White to off-white crystalline powder
Solubility
Soluble in organic solvents, insoluble in water
Application
Research and development of pharmaceuticals
Relevance
Study of neurological disorders and potential treatments
Check Digit Verification of cas no
The CAS Registry Mumber 1311314-54-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,3,1 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1311314-54:
(9*1)+(8*3)+(7*1)+(6*1)+(5*3)+(4*1)+(3*4)+(2*5)+(1*4)=91
91 % 10 = 1
So 1311314-54-1 is a valid CAS Registry Number.
1311314-54-1Relevant articles and documents
An efficient synthesis of 1-methyl-4,5,6,7-tetrahydro-1 H-pyrrolo[2,3-c]pyridine and its N6-substituted analogues
Nechayev, Maxim A.,Gorobets, Nikolay Yu.,Kovalenko, Sergiy M.,Tolmachev, Andrey A.
, p. 919 - 924 (2013)
An efficient synthesis of 1-methyl-4,5,6,7-tetrahydro-1H-pyrrolo[2,3-c] pyridine hydrochloride was achieved using simple sodium borohydride reduction of 6-benzyl-1-methyl-1H-pyrrolo[2,3-c]pyridin-6-ium bromide as the key step followed by its debenzylation with hydrogen over palladium on carbon on a multigram scale. Similarly, a series of N6-substituted 1-methyl-1H-pyrrolo[2,3-c]pyridin-6-ium halides were synthesized and reduced with sodium borohydride, showing this method to be applicable for the synthesis of different N6-substituted 1-methyl-4,5,6,7-tetrahydro-1H-pyrrolo[2, 3-c]pyridines. Georg Thieme Verlag Stuttgart - New York.
