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Catalog Number:
29586
CAS Number:
163705-28-0
R-Boc-2-amino-3-phenylsulfanyl-propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Cys(phenyl)-OH
Documents
$134.70 /100MG
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Product Information

(R)-Boc-2-amino-3-phenylsulfanyl-propionic acid is a valuable compound in the field of organic synthesis and medicinal chemistry. This chiral amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and usability in various chemical reactions. Its unique structure, characterized by the presence of a phenylsulfanyl group, makes it an excellent candidate for the development of novel pharmaceuticals and bioactive compounds. Researchers utilize this compound in the synthesis of peptide-based drugs and as a building block for more complex molecules, particularly in the design of inhibitors and other therapeutic agents.

The compound's ability to act as a versatile intermediate allows for the exploration of diverse chemical pathways, making it a preferred choice for professionals in drug discovery and development. Its favorable properties, including solubility and reactivity, further support its application in various research settings. With its potential to contribute to advancements in medicinal chemistry, (R)-Boc-2-amino-3-phenylsulfanyl-propionic acid stands out as a key resource for scientists aiming to innovate in therapeutic solutions.

Synonyms
Boc-L-Cys(phenyl)-OH
CAS Number
163705-28-0
Purity
≥ 99% (HPLC)
Molecular Formula
C14H19NO4S
Molecular Weight
297.37
MDL Number
MFCD08063988
PubChem ID
14796017
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -39 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Cys(phenyl)-OH
CAS Number
163705-28-0
Purity
≥ 99% (HPLC)
Molecular Formula
C14H19NO4S
Molecular Weight
297.37
MDL Number
MFCD08063988
PubChem ID
14796017
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -39 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-Boc-2-amino-3-phenylsulfanyl-propionic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it can enhance the stability and efficacy of drug candidates.
  • Drug Development: Its unique structure allows for the design of novel therapeutics targeting specific biological pathways, making it essential in the development of new medications.
  • Bioconjugation: The compound can be used in bioconjugation processes to attach drugs or imaging agents to biomolecules, improving the delivery and targeting of therapies in cancer treatment.
  • Research in Neuroscience: It has applications in neuroscience research, particularly in studying neurotransmitter systems, due to its ability to modulate certain receptor activities.
  • Analytical Chemistry: This chemical is also employed in analytical methods for detecting and quantifying amino acids in biological samples, aiding researchers in metabolic studies.

Citations