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Catalog Number:
19654
CAS Number:
1187933-37-4
Ester tert -butylique de l'acide S- (1,2,3,4-tétrahydroisoquinolin-3-yl-méthyl)carbamique
Synonym(s):
( S -3-Boc-aminométhyl-1,2,3,4-tétrahydroisoquinoléine
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Product Information

(S)-(1,2,3,4-Tetrahydroisoquinolin-3-yl-methyl)carbamic acid tert-butyl ester is a versatile compound with significant potential in pharmaceutical research and development. This compound, also known as tert-butyl N-[[(3S)-1,2,3,4-tetrahydroisoquinolin-3-yl]methyl]carbamate, features a unique structure that allows for various applications, particularly in the synthesis of bioactive molecules. Its ability to act as a building block in medicinal chemistry makes it an attractive option for researchers focused on developing new therapeutic agents targeting neurological disorders and other health conditions.

The tert-butyl ester group enhances the compound's solubility and stability, making it suitable for various formulations. Its specific stereochemistry contributes to its biological activity, which can be leveraged in drug design and development. Researchers can utilize this compound in the exploration of novel treatments, particularly in areas such as neuropharmacology, where its derivatives may exhibit promising effects. With its unique properties and potential applications, this compound stands out as a valuable asset for professionals in the pharmaceutical and chemical industries.

Synonyms
( S -3-Boc-aminométhyl-1,2,3,4-tétrahydroisoquinoléine
CAS Number
1187933-37-4
Molecular Formula
C15H22N2O2
Molecular Weight
262.35
MDL Number
MFCD06804517
PubChem ID
42614617
Conditions
Conserver à 0-8°C
General Information
Synonyms
( S -3-Boc-aminométhyl-1,2,3,4-tétrahydroisoquinoléine
CAS Number
1187933-37-4
Molecular Formula
C15H22N2O2
Molecular Weight
262.35
MDL Number
MFCD06804517
PubChem ID
42614617
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-(1,2,3,4-Tetrahydroisoquinolin-3-yl-methyl)carbamic acid tert-butyl ester 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.
  • Neuroscience Research: It is used in studies investigating the mechanisms of action of neurotransmitters, helping researchers understand brain function and potential treatments for mental health conditions.
  • Drug Delivery Systems: The compound's unique properties allow it to be incorporated into drug delivery systems, enhancing the bioavailability and efficacy of therapeutic agents.
  • Organic Synthesis: It acts as a versatile building block in organic synthesis, facilitating the creation of complex molecules in a more efficient manner compared to traditional methods.
  • Biochemical Assays: Researchers utilize this compound in biochemical assays to evaluate enzyme activity and interactions, providing valuable insights into metabolic pathways.

Citations