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Catalog Number:
31686
CAS Number:
109517-87-5
Boc-L-Lys(2-Cl-Z)-O-CH2-Ph-CH2-COOH
Purity:
≥ 98% (HPLC)
Documents
$208.31 /1G
Pack Size Availability Price
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Product Information

Boc-L-Lys(2-Cl-Z)-O-CH2-Ph-CH2-COOH is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This protected lysine derivative features a Boc (tert-butyloxycarbonyl) group, which provides stability during synthesis and facilitates the selective deprotection of the amino group when needed. The presence of a chlorophenyl moiety enhances its reactivity, making it an excellent candidate for coupling reactions in the formation of complex peptides. Researchers often leverage this compound in the development of therapeutic peptides, particularly in the fields of drug design and delivery systems, due to its ability to improve solubility and bioavailability.

In addition to its applications in peptide synthesis, Boc-L-Lys(2-Cl-Z)-O-CH2-Ph-CH2-COOH is also valuable in the study of protein interactions and enzyme activity. Its unique structure allows for modifications that can lead to the development of novel biomolecules with enhanced properties. This compound stands out among similar products due to its specific functional groups, which can be tailored for various applications in medicinal chemistry and biochemistry, making it an essential tool for researchers aiming to innovate in their respective fields.

CAS Number
109517-87-5
Purity
≥ 98% (HPLC)
Molecular Formula
C28H35ClN2O8
Molecular Weight
563.05
MDL Number
MFCD00273505
PubChem ID
155894539
Melting Point
66-72 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -17 ± 2° (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
109517-87-5
Purity
≥ 98% (HPLC)
Molecular Formula
C28H35ClN2O8
Molecular Weight
563.05
MDL Number
MFCD00273505
PubChem ID
155894539
Melting Point
66-72 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -17 ± 2° (C=1 in EtOH)
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

Boc-L-Lys(2-Cl-Z)-O-CH2-Ph-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its protective groups allow for selective reactions, enhancing yield and purity.
  • Drug Development: It is used in the design of novel pharmaceuticals, especially in oncology and immunology, where modified peptides can improve efficacy and reduce side effects.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking drugs to antibodies or other biomolecules, which can enhance targeting and delivery in treatments.
  • Research in Molecular Biology: It aids in studying protein interactions and functions, providing insights into cellular mechanisms that can lead to breakthroughs in disease understanding.
  • Custom Synthesis Services: Companies specializing in custom chemical synthesis utilize this compound to create tailored solutions for clients in pharmaceuticals and biotechnology, addressing specific research needs.

Citations