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Catalog Number:
07334
CAS Number:
221352-46-1
Acide Boc-( R , S -1,3-dihydro-2 H -isoindole carboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Disque Boc-DL-OH
Documents
$100.05 /250 mg
Taille
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Product Information

Boc-(R,S)-1,3-dihydro-2H-isoindole 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 choice for various applications in peptide synthesis and medicinal chemistry. Its unique structure allows for the selective modification of functional groups, facilitating the development of novel bioactive molecules. Researchers often leverage this compound in the synthesis of isoindole derivatives, which have shown promising biological activities, including anti-inflammatory and anticancer properties.

In addition to its role in synthetic chemistry, Boc-(R,S)-1,3-dihydro-2H-isoindole carboxylic acid serves as a valuable intermediate in the preparation of complex organic compounds. Its ability to undergo various transformations while maintaining structural integrity makes it a preferred choice among chemists. This compound not only streamlines the synthesis process but also enhances the efficiency of developing new therapeutic agents, thereby holding significant potential for advancing drug discovery and development.

Synonyms
Disque Boc-DL-OH
CAS Number
221352-46-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 14 H 17 NON 4
Molecular Weight
263.31
MDL Number
MFCD01321007
PubChem ID
2755967
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Disque Boc-DL-OH
CAS Number
221352-46-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 14 H 17 NON 4
Molecular Weight
263.31
MDL Number
MFCD01321007
PubChem ID
2755967
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(R,S)-1,3-dihydro-2H-isoindole carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Peptide Synthesis: Its protective Boc (tert-butyloxycarbonyl) group is advantageous in peptide synthesis, allowing for selective deprotection and facilitating the formation of complex peptide structures.
  • Organic Synthesis: The compound is employed in organic synthesis as a building block for creating diverse chemical entities, enhancing the efficiency of multi-step reactions.
  • Material Science: It finds applications in the development of new materials, particularly in the creation of polymers with unique properties, which can be tailored for specific applications.
  • Research in Medicinal Chemistry: Researchers leverage this compound to explore new therapeutic agents, benefiting from its structural features that can lead to improved bioactivity and selectivity.

Citations