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Catalog Number:
22706
CAS Number:
1031927-09-9
R,S)-Boc-Thc(Boc)-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido (R,S)-3-Boc-amino-9-Boc-1,2,3,4-tetrahidro-carbazol-3-carboxílico
Documents
$72.31 /100 mg
Tamaño
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Product Information

(R,S)-Boc-Thc(Boc)-OH is a versatile compound widely utilized in pharmaceutical and chemical research, particularly in the synthesis of complex organic molecules. This compound, also known as 9-[(2-methylpropan-2-yl)oxycarbonyl]-3-[(2-methylpropan-2-yl)oxycarbonylamino]-2,4-dihydro-1H-carbazole-3-carboxylic acid, features protective Boc (tert-butyloxycarbonyl) groups that enhance its stability and reactivity, making it an excellent choice for peptide synthesis and drug development. Its unique structure allows for selective reactions, facilitating the creation of intricate molecular architectures that are essential in medicinal chemistry.

Researchers and industry professionals appreciate (R,S)-Boc-Thc(Boc)-OH for its ability to streamline synthetic pathways and improve yields in complex reactions. Its applications extend to the development of novel therapeutics, where it serves as a key intermediate in the synthesis of bioactive compounds. The compound's favorable properties, such as its solubility and compatibility with various reaction conditions, make it a valuable asset in laboratories focused on drug discovery and development.

Synonyms
Ácido (R,S)-3-Boc-amino-9-Boc-1,2,3,4-tetrahidro-carbazol-3-carboxílico
CAS Number
1031927-09-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H30N2O6
Molecular Weight
430.5
MDL Number
MFCD09264203
PubChem ID
44118853
Melting Point
160-174 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido (R,S)-3-Boc-amino-9-Boc-1,2,3,4-tetrahidro-carbazol-3-carboxílico
CAS Number
1031927-09-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H30N2O6
Molecular Weight
430.5
MDL Number
MFCD09264203
PubChem ID
44118853
Melting Point
160-174 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R,S)-Boc-Thc(Boc)-OH is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without unwanted reactions, which is crucial in developing new pharmaceuticals.
  • Drug Development: Its role in drug formulation helps enhance the solubility and stability of active pharmaceutical ingredients, making it valuable in the pharmaceutical industry for creating effective medications.
  • Biotechnology: Researchers use this compound in the production of biologically active compounds, aiding in the development of novel therapeutics and biocatalysts that can address various health challenges.
  • Organic Synthesis: It is a key intermediate in organic synthesis, facilitating the creation of complex molecules that are essential in materials science and chemical research.
  • Research Applications: The compound is frequently employed in academic and industrial research settings to explore new chemical reactions and pathways, contributing to advancements in chemistry and related fields.

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