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Catalog Number:
17893
CAS Number:
123811-87-0
Acide 1-Boc-1,2,3,4-tétrahydroquinoléine-2-carboxylique
Purity:
≥ 97 % (dosage)
Synonym(s):
Acide 1-Boc-3,4-dihydro-2 H -quinoléine-2-carboxylique, Acide 3,4-dihydro-2 H -quinoléine-1,2-dicarboxylique 1 -tert -butyl ester
Documents
$127.79 /250 mg
Taille
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Product Information

1-Boc-1,2,3,4-tetrahydroquinoline-2-carboxylic acid is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal intermediate in the synthesis of various bioactive molecules. Its unique structure allows for the development of novel pharmaceuticals, particularly in the fields of neuropharmacology and medicinal chemistry, where it can serve as a building block for the creation of compounds targeting neurological disorders.

Researchers appreciate 1-Boc-1,2,3,4-tetrahydroquinoline-2-carboxylic acid for its ability to facilitate complex reactions while maintaining high yields. Its applications extend to the synthesis of heterocyclic compounds, which are crucial in drug development. Additionally, the compound's favorable properties, such as solubility and stability under various conditions, make it a preferred choice for laboratories focused on innovative drug discovery and development.

Synonyms
Acide 1-Boc-3,4-dihydro-2 H -quinoléine-2-carboxylique, Acide 3,4-dihydro-2 H -quinoléine-1,2-dicarboxylique 1 -tert -butyl ester
CAS Number
123811-87-0
Purity
≥ 97 % (dosage)
Molecular Formula
C 15 H 19 NON 4
Molecular Weight
277.32
MDL Number
MFCD04115277
PubChem ID
19823205
Appearance
Solide jaunâtre
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide 1-Boc-3,4-dihydro-2 H -quinoléine-2-carboxylique, Acide 3,4-dihydro-2 H -quinoléine-1,2-dicarboxylique 1 -tert -butyl ester
CAS Number
123811-87-0
Purity
≥ 97 % (dosage)
Molecular Formula
C 15 H 19 NON 4
Molecular Weight
277.32
MDL Number
MFCD04115277
PubChem ID
19823205
Appearance
Solide jaunâtre
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1-Boc-1,2,3,4-tetrahydroquinoline-2-carboxylic acid is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its structural similarity to bioactive molecules.
  • Drug Development: It is used in the development of novel drugs, especially in the creation of compounds that can cross the blood-brain barrier, enhancing therapeutic efficacy for central nervous system diseases.
  • Biochemical Research: Researchers employ this compound to study enzyme interactions and metabolic pathways, providing insights into cellular processes and potential therapeutic targets.
  • Material Science: Its unique properties make it useful in the formulation of advanced materials, such as polymers and coatings, which require specific chemical characteristics for improved performance.
  • Analytical Chemistry: This compound is utilized in various analytical techniques, including chromatography and spectroscopy, to identify and quantify related compounds in complex mixtures.

Citations