70291-26-8 Usage
Description
2-Chloro-3-pyrrol-1-ylpyridine is an organic compound characterized by its unique molecular structure, which features a pyridine ring fused with a pyrrole ring and a chlorine atom at the 2nd position. 2-CHLORO-3-PYRROL-1-YLPYRIDINE is known for its potential applications in the synthesis of various complex organic molecules and pharmaceuticals.
Uses
Used in Pharmaceutical Synthesis:
2-Chloro-3-pyrrol-1-ylpyridine is used as a key reactant for the synthesis of pyrido[2,3-e]pyrrolo[1,2-a]pyrazine derivatives. These derivatives are important in the development of new pharmaceutical compounds due to their diverse biological activities and potential therapeutic applications.
Used in Organic Chemistry Research:
In the field of organic chemistry, 2-chloro-3-pyrrol-1-ylpyridine serves as a valuable building block for the creation of novel molecular structures. Its unique fusion of pyridine and pyrrole rings, along with the chlorine atom, allows for further functionalization and exploration of new chemical reactions and pathways.
Used in Material Science:
2-CHLORO-3-PYRROL-1-YLPYRIDINE may also find applications in material science, particularly in the development of new materials with specific properties. The unique structure of 2-chloro-3-pyrrol-1-ylpyridine can be utilized to create new polymers, dyes, or other materials with tailored characteristics for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 70291-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,9 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70291-26:
(7*7)+(6*0)+(5*2)+(4*9)+(3*1)+(2*2)+(1*6)=108
108 % 10 = 8
So 70291-26-8 is a valid CAS Registry Number.
70291-26-8Relevant articles and documents
Synthesis of pyrido[2,3-e]pyrrolo[1,2-a]pyrazine derivatives via tandem iminium cyclization and smiles rearrangement
Xiang, Jinbao,Xie, Hongxiang,Wen, Dongsheng,Dang, Qun,Bai, Xu
, p. 3281 - 3283 (2008/09/19)
(Chemical Equation Presented) The tandem iminium cyclization and Smiles rearrangement of pyridinyloxyacetaldehyde 1 and a primary amine generated a novel pyrido[2,3-e]pyrrolo[1,2-a]pyrazine scaffold. TFA was discovered to be an efficient catalyst in the r
REINVESTIGATION OF A CYCLIZATION REACTION OF 2-HYDRAZINO-3-(1H-PYRROL-1-YL)PYRIDINE
Peet, Norton P.,Sunder, Shyam
, p. 3213 - 3221 (2007/10/02)
The reaction of 2-hydrazino-3-(1H-pyrrol-1-yl)pyridine (3) with acetylacetone affords 2-(3,5-dimethyl-1H-pyrazol-1-yl)-3-(1H-pyrrol-1-yl)pyridine (7) rather than 3,5-dimethyl-10-(1H-pyrrol-1-yl)pyridotriazepine (5), as previously reported.
Heterocycle substituted (3-loweralkylamino-2-R1 O-propoxy)pyridines
-
, (2008/06/13)
Heterocycle substituted (3-loweralkylamino-2-R1 O-propoxy)pyridines, their pharmaceutically acceptable salts and their preparation are disclosed. These pyridines have pharmaceutical properties such as anti-hypertensive activity of rapid onset.