Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
12373
CAS Number:
41994-51-8
Ácido R , S ,-1,2,3,4-tetrahidro-3-isoquinolincarboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
DL-Tic-OH
Documents
$86.23 /1G
Tamaño
Request Bulk Quote
Product Information

(R,S)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid is a versatile compound with significant applications in pharmaceutical research and development. This compound is recognized for its role as a building block in the synthesis of various bioactive molecules, particularly in the development of drugs targeting neurological disorders. Its unique structure allows for modifications that can enhance biological activity, making it a valuable asset in medicinal chemistry. Researchers have utilized this compound in studies related to neurotransmitter modulation, showcasing its potential in treating conditions such as depression and anxiety.

Additionally, (R,S)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid serves as a chiral intermediate in the synthesis of other complex organic compounds, which is crucial in the production of enantiomerically pure substances. Its ability to facilitate the creation of diverse chemical entities underscores its importance in both academic and industrial settings. With its favorable properties and broad applicability, this compound stands out as a key ingredient for researchers and professionals aiming to innovate in drug development and organic synthesis.

Synonyms
DL-Tic-OH
CAS Number
41994-51-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H11NO2
Molecular Weight
177.2
MDL Number
MFCD00191496
PubChem ID
2724135
Melting Point
258-262 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
DL-Tic-OH
CAS Number
41994-51-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H11NO2
Molecular Weight
177.2
MDL Number
MFCD00191496
PubChem ID
2724135
Melting Point
258-262 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R,S)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Neuroprotective Research: Its unique structure allows researchers to explore its potential neuroprotective effects, making it valuable in studies related to neurodegenerative diseases.
  • Analytical Chemistry: The compound is used in analytical methods to develop new techniques for detecting and quantifying isoquinoline derivatives, aiding in quality control processes.
  • Biochemical Studies: It acts as a tool in biochemical research to investigate enzyme interactions and metabolic pathways, providing insights into cellular functions.
  • Material Science: The compound is explored for its potential applications in creating novel materials, such as polymers with specific mechanical properties, expanding its utility beyond traditional chemistry.

Citas