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Catalog Number:
47476
CAS Number:
143112-49-6
( R )-(-)-4-( N , N -Diméthylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
Purity:
≥ 98 % (HPLC)
Synonym(s):
( R )-(-)-4-( N , N -Diméthylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)benzofurazane, ( R )-(-)-4-( N , N -Diméthylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
Documents
$218.40 /100 mg
Taille
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Product Information

(R)-(-)-4-(N,N-Dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole is a specialized compound known for its unique sulfonamide structure, which enhances its reactivity and solubility in various solvents. This compound is particularly valuable in pharmaceutical research and development, where it serves as a key intermediate in the synthesis of biologically active molecules. Its ability to interact with biological systems makes it a promising candidate for drug discovery, especially in the fields of neuropharmacology and medicinal chemistry. Researchers have utilized this compound to explore its potential in developing treatments for neurological disorders, leveraging its structural properties to design effective therapeutic agents.

Additionally, the compound's distinctive features, such as its chiral center, allow for the exploration of stereochemistry in drug design, which can lead to improved efficacy and reduced side effects in pharmaceutical applications. Its versatility in synthetic pathways makes it an essential tool for chemists aiming to innovate in drug formulation and development. With its robust profile, (R)-(-)-4-(N,N-Dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole stands out as a valuable asset for researchers and industry professionals focused on advancing medicinal chemistry.

Synonyms
( R )-(-)-4-( N , N -Diméthylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)benzofurazane, ( R )-(-)-4-( N , N -Diméthylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
CAS Number
143112-49-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H17N5O3S
Molecular Weight
311.36
MDL Number
MFCD00191379
PubChem ID
5146819
Melting Point
128 - 132 °C
Appearance
Poudre jaune pâle à brune
Optical Rotation
[a]20/D = -3 à -7 ° (C=1 dans l'acétonitrile)
Conditions
Conserver entre 2 et 8 °C, sous gaz inerte.
General Information
Synonyms
( R )-(-)-4-( N , N -Diméthylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)benzofurazane, ( R )-(-)-4-( N , N -Diméthylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
CAS Number
143112-49-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H17N5O3S
Molecular Weight
311.36
MDL Number
MFCD00191379
PubChem ID
5146819
Melting Point
128 - 132 °C
Appearance
Poudre jaune pâle à brune
Optical Rotation
[a]20/D = -3 à -7 ° (C=1 dans l'acétonitrile)
Conditions
Conserver entre 2 et 8 °C, sous gaz inerte.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(R)-(-)-4-(N,N-Dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of new drugs, particularly in the development of treatments for neurological disorders due to its ability to interact with specific receptors in the brain.
  • Biochemical Research: It is employed in studies investigating enzyme activity and protein interactions, helping researchers understand complex biological processes and develop targeted therapies.
  • Analytical Chemistry: The compound is used as a reagent in various analytical methods, including fluorescence spectroscopy, allowing for sensitive detection of biomolecules in complex samples.
  • Material Science: Its unique properties make it suitable for creating advanced materials, such as sensors and polymers, that respond to environmental changes, enhancing the functionality of devices.
  • Diagnostics: This chemical is being explored for use in diagnostic assays, where its specificity can improve the accuracy of tests for various diseases, providing better patient outcomes.

Citations