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Catalog Number:
11889
CAS Number:
327603-46-3
Ácido Boc- N en -formil-L-1,2,3,4-tetrahidronorharmano-3-carboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Tpi(Para)-OH
Documents
$52.10 /1G
Tamaño
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Product Information

Boc-Nin-formyl-L-1,2,3,4-tetrahydronorharmane-3-carboxylic acid is a versatile compound that plays a significant role in organic synthesis and pharmaceutical research. This compound, characterized by its unique structure, is particularly valuable in the development of novel therapeutic agents. Its ability to serve as a building block in the synthesis of complex molecules makes it an essential tool for researchers focused on drug discovery and development. The presence of the Boc (tert-butyloxycarbonyl) protecting group enhances its stability and reactivity, allowing for selective reactions in multi-step synthesis processes.

In addition to its applications in medicinal chemistry, Boc-Nin-formyl-L-1,2,3,4-tetrahydronorharmane-3-carboxylic acid is also utilized in the study of neuroactive compounds, contributing to the understanding of various neurological pathways. Its unique properties make it an attractive candidate for further exploration in the fields of biochemistry and pharmacology, where it can aid in the design of innovative treatments for neurological disorders. Researchers and industry professionals will find this compound to be a valuable asset in their work, offering both versatility and potential for groundbreaking discoveries.

Synonyms
Boc-L-Tpi(Para)-OH
CAS Number
327603-46-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C18H20N2O5
Molecular Weight
344.35
MDL Number
MFCD01862297
PubChem ID
75627274
Melting Point
113-125 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[α] D 20 = +81 ± 2º (C=1 en EtOAc)
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
Synonyms
Boc-L-Tpi(Para)-OH
CAS Number
327603-46-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C18H20N2O5
Molecular Weight
344.35
MDL Number
MFCD01862297
PubChem ID
75627274
Melting Point
113-125 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[α] D 20 = +81 ± 2º (C=1 en EtOAc)
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

Boc-Nin-formyl-L-1,2,3,4-tetrahydronorharmane-3-carboxylic acid is widely utilized in research focused on:

  • Synthesis of Bioactive Compounds: This chemical serves as a key intermediate in the synthesis of various bioactive molecules, particularly in pharmaceutical research, aiding in the development of new drugs.
  • Peptide Chemistry: It is used in peptide synthesis, where its protective group facilitates the formation of peptide bonds, making it easier to manipulate amino acids without unwanted reactions.
  • Medicinal Chemistry: Researchers employ this compound to explore its potential therapeutic effects, particularly in neuropharmacology, due to its structural similarities to known psychoactive substances.
  • Analytical Chemistry: The compound is utilized in analytical methods to study the behavior of complex organic molecules, providing insights into their stability and reactivity under various conditions.
  • Material Science: It finds applications in the development of novel materials with specific properties, such as polymers or coatings, benefiting industries focused on advanced materials.

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