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Catalog Number:
15347
CAS Number:
270062-98-1
Boc-(S-2-tetrahydroisoquinoline acetic acid
Purity:
≥ 97% (Assay)
Synonym(s):
Boc-(S)-2-tetrahydroisoquinoline acetic acid, Boc-(S-1,2,3,4-tetrahydroisoquinoline-3-acetic acid
Documents
$101.75 /100MG
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Product Information

Boc-(S)-2-tetrahydroisoquinoline acetic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound serves as a crucial building block in the development of various pharmaceuticals, particularly in the synthesis of isoquinoline derivatives, which are known for their diverse biological activities. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, enhances its stability and reactivity, making it an ideal candidate for complex organic transformations. Researchers appreciate its role in the synthesis of potential therapeutic agents, including those targeting neurological disorders and cancer.

In addition to its applications in drug development, Boc-(S)-2-tetrahydroisoquinoline acetic acid is also valuable in the production of chiral intermediates, which are essential in the formulation of enantiomerically pure compounds. Its ability to facilitate asymmetric synthesis provides a significant advantage over other similar compounds, allowing for more efficient and selective reactions. This compound is a must-have for researchers and industry professionals looking to innovate in the fields of pharmaceuticals and fine chemicals.

Synonyms
Boc-(S)-2-tetrahydroisoquinoline acetic acid, Boc-(S-1,2,3,4-tetrahydroisoquinoline-3-acetic acid
CAS Number
270062-98-1
Purity
≥ 97% (Assay)
Molecular Formula
C16H21NO4
Molecular Weight
291.35
MDL Number
MFCD01861031
PubChem ID
50851982
Appearance
White solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-(S)-2-tetrahydroisoquinoline acetic acid, Boc-(S-1,2,3,4-tetrahydroisoquinoline-3-acetic acid
CAS Number
270062-98-1
Purity
≥ 97% (Assay)
Molecular Formula
C16H21NO4
Molecular Weight
291.35
MDL Number
MFCD01861031
PubChem ID
50851982
Appearance
White solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-2-tetrahydroisoquinoline acetic acid is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Building Blocks: It is an important chiral building block used in asymmetric synthesis, allowing for the creation of compounds with specific stereochemistry, which is crucial in drug development.
  • Research in Medicinal Chemistry: The compound is employed in medicinal chemistry research to explore new therapeutic agents, particularly those that require isoquinoline derivatives for enhanced biological activity.
  • Bioconjugation Applications: It can be used in bioconjugation processes, facilitating the attachment of drugs to biomolecules, which can improve drug delivery and efficacy.
  • Development of Novel Materials: Researchers utilize this compound in the development of novel materials with unique properties, including polymers and nanomaterials, enhancing their performance in various applications.

Citations