161553-18-0

Basic information

• Product Name: (S)- ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID
• Synonyms: (S)- ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID;(S)-2-AMino-3-(6-chloroiMidazo[1,2-b]pyridazin-2-yl)propanoic acid
• CAS NO: 161553-18-0
• Molecular Formula: C9H9 Cl N4 O2
• Molecular Weight: 240.65
• Mol File: 161553-18-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (S)- ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (S)- ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID(161553-18-0)
• EPA Substance Registry System: (S)- ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID(161553-18-0)

Safety Data

• Hazardous Substances Data: 161553-18-0(Hazardous Substances Data)

Usage

Description

(S)ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID is a chemical compound characterized by an imidazo[1,2-b]pyridazine ring with a chlorine atom at the 6th position, an amino group at the alpha carbon, and a propanoic acid group attached at the 2nd position. (S)ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID holds potential pharmaceutical applications due to its unique structure, which may enable interactions with specific biological targets in the body. Its properties could be harnessed in the development of medications for various conditions, although further research and testing are necessary to comprehend its full potential uses and effects.

Uses

Used in Pharmaceutical Industry:
(S)ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID is used as a potential pharmaceutical compound for its ability to interact with biological targets. Its unique structure may allow it to be developed into medication for certain conditions, pending further research and testing to confirm its efficacy and safety.
Used in Research and Development:
In the field of scientific research, (S)ALPHA-AMINO-6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-2-PROPANOIC ACID serves as a subject for exploration and experimentation. It is used as a chemical probe to study its interactions with biological systems and to understand its potential applications in drug development and therapeutic interventions.

Upstream product

• 161659-60-5 (R)-N-trifluoroacetyl-5-diazo-4-oxonorvaline methyl ester 
• 161553-10-2 (R)-N-trifluoroacetyl-5-bromo-4-oxonorvaline methyl ester 
• 161553-15-7 (R)-trifluoroacetyl-3-(6-chloroimidazo<1,2-b>pyridazin-2-yl)alanine methyl ester 
• 161553-09-9 methyl (2S)-5-bromo-4-oxo-2-(2,2,2-trifluoroacetamido)-pentanoate 
• 88668-76-2 methyl (2S)-5-diazo-4-oxo-2-(2,2,2-trifluoroacetamido)-pentanoate 
• 161553-14-6 (S)-trifluoroacetyl-3-(6-chloroimidazo<1,2-b>pyridazin-2-yl)alanine methyl ester 
• 188621-34-3 (R,S)-N-trifluoroacetyl-5-bromo-4-oxonorvaline methyl ester 
• 161659-61-6 (R,S)-N-trifluoroacetyl-5-diazo-4-oxonorvaline methyl ester 
• 161659-62-7 (R,S)-trifluoroacetyl-3-(6-chloroimidazo<1,2-b>pyridazin-2-yl)alanine methl ester 

Relevant articles and documents

The synthesis of azatryptophane derivatives

Optically active and racemic isomers of aspartic acid (1) were transformed into the corresponding N-trifluoroacetyl-5-bromo-4-oxonorvaline methyl esters (6, R = Me) and N-trifluoroacetyl-3-formylalanine methyl esters 13, which were used as starting compou