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Catalog Number:
24337
CAS Number:
143262-20-8
1-(tert-Butoxycarbonyl)indoline-7-carboxylic acid
Purity:
≥ 99.9% (HPLC)
Synonym(s):
2,3-Dihydro-indole-1,7-dicarboxylic acid 1-tert-butyl ester
Documents
$173.66 /250MG
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Product Information

1-(tert-Butoxycarbonyl)indoline-7-carboxylic acid is a versatile compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is particularly advantageous in organic synthesis, allowing for selective reactions while maintaining the integrity of sensitive functional groups. Its unique structure makes it an essential building block in the development of indole-based derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties.

Researchers and industry professionals appreciate this compound for its stability and ease of handling, making it suitable for both laboratory and industrial applications. Its role in the synthesis of complex molecules underscores its importance in medicinal chemistry, where it can facilitate the creation of novel therapeutic agents. Additionally, the compound's ability to undergo various transformations enhances its utility in the development of innovative solutions across multiple sectors, including pharmaceuticals and agrochemicals.

Synonyms
2,3-Dihydro-indole-1,7-dicarboxylic acid 1-tert-butyl ester
CAS Number
143262-20-8
Purity
≥ 99.9% (HPLC)
Molecular Formula
C14H17NO4
Molecular Weight
263.29
MDL Number
MFCD04973983
PubChem ID
14977845
Appearance
Off-white solid
Conditions
Store at 0-8°C
General Information
Synonyms
2,3-Dihydro-indole-1,7-dicarboxylic acid 1-tert-butyl ester
CAS Number
143262-20-8
Purity
≥ 99.9% (HPLC)
Molecular Formula
C14H17NO4
Molecular Weight
263.29
MDL Number
MFCD04973983
PubChem ID
14977845
Appearance
Off-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

1-(tert-Butoxycarbonyl)indoline-7-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 novel drugs targeting neurological disorders.
  • Organic Synthesis: It is used in organic chemistry for the preparation of indoline derivatives, which are important in creating complex molecules with diverse biological activities.
  • Biotechnology: The compound plays a role in the production of peptide-based therapeutics, providing a protective group that enhances the stability and solubility of peptides during synthesis.
  • Material Science: Its unique properties make it suitable for developing advanced materials, including polymers and coatings that require specific chemical functionalities.
  • Research in Medicinal Chemistry: This chemical is valuable in exploring structure-activity relationships (SAR) in drug design, helping researchers understand how modifications can enhance efficacy and reduce side effects.

Citations