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Catalog Number:
29629
CAS Number:
1354752-83-2
( Acide S -Boc-3-benzyl-pipéridine-3-carboxylique·DCHA
Purity:
≥ 99 % (HPLC)
Documents
$168.35 /100 mg
Taille
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Product Information

(S)-Boc-3-benzyl-piperidine-3-carboxylic acid·DCHA is a versatile compound widely utilized in the pharmaceutical and chemical research sectors. This compound features a unique structure that includes a benzyl group and a Boc (tert-butyloxycarbonyl) protecting group, making it an excellent candidate for various synthetic applications. Its ability to serve as an intermediate in the synthesis of bioactive molecules enhances its relevance in drug discovery and development. Researchers appreciate its stability and ease of handling, which facilitate efficient reactions in complex organic syntheses.

In addition to its synthetic utility, (S)-Boc-3-benzyl-piperidine-3-carboxylic acid·DCHA is particularly valuable in the development of piperidine derivatives, which are integral to many therapeutic agents. Its application extends to the creation of compounds with potential analgesic and anti-inflammatory properties, showcasing its importance in medicinal chemistry. With its favorable characteristics, this compound stands out as a reliable choice for professionals seeking to innovate in drug formulation and organic synthesis.

CAS Number
1354752-83-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 18 H 25 NO 4 · C 12 H 23 N
Molecular Weight
500.72
MDL Number
MFCD26793604
PubChem ID
167994284
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -22 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
CAS Number
1354752-83-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 18 H 25 NO 4 · C 12 H 23 N
Molecular Weight
500.72
MDL Number
MFCD26793604
PubChem ID
167994284
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -22 ± 2º (C = 1 dans DMF)
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)-Boc-3-benzyl-piperidine-3-carboxylic acid·DCHA 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 analgesics and anti-inflammatory drugs.
  • Organic Synthesis: It is employed in organic chemistry as a building block for creating complex molecules, facilitating the design of new compounds with specific biological activities.
  • Neuroscience Research: Researchers use this compound to study its effects on neurotransmitter systems, which can lead to advancements in treatments for neurological disorders.
  • Drug Formulation: The compound's unique properties allow it to enhance the solubility and stability of drug formulations, improving their efficacy and shelf life.
  • Chiral Synthesis: As a chiral molecule, it plays a crucial role in asymmetric synthesis, which is essential for producing enantiomerically pure compounds in the pharmaceutical industry.

Citations