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Catalog Number:
11935
CAS Number:
56787-36-1
Chloroacetyl-L-norleucine
Purity:
≥ 99%
Synonym(s):
ClAc-L-Nle-OH, Chloroacetyl-L-2-aminohexanoic acid
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$30.35 /1G
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Product Information

Chloroacetyl-L-norleucine is a versatile compound that plays a significant role in various fields, particularly in pharmaceutical and biochemical research. This amino acid derivative is recognized for its unique structure, which includes a chloroacetyl group that enhances its reactivity and potential applications. Researchers often utilize Chloroacetyl-L-norleucine in the synthesis of peptide-based drugs, where its ability to modify peptide chains can lead to improved pharmacological properties. Its reactivity allows for the introduction of specific functionalities in drug design, making it a valuable tool for medicinal chemists.

In addition to its applications in drug development, Chloroacetyl-L-norleucine is also explored in the study of protein interactions and enzyme activity. Its incorporation into various biochemical assays can provide insights into metabolic pathways and protein function. With its favorable properties, this compound stands out as a crucial ingredient for researchers aiming to innovate in therapeutic formulations and biochemical studies. The potential for enhanced efficacy in drug design and the ability to elucidate complex biological mechanisms make Chloroacetyl-L-norleucine an essential asset in modern scientific research.

Synonyms
ClAc-L-Nle-OH, Chloroacetyl-L-2-aminohexanoic acid
CAS Number
56787-36-1
Purity
≥ 99%
Molecular Formula
C8H14NO3Cl
Molecular Weight
207.65
MDL Number
MFCD00190854
PubChem ID
306113
Melting Point
67-72 ºC
Appearance
White powder
Optical Rotation
[a]D20 = -16 ± 2º (C=2 in H2O)
Conditions
Store at 0-8°C
General Information
Synonyms
ClAc-L-Nle-OH, Chloroacetyl-L-2-aminohexanoic acid
CAS Number
56787-36-1
Purity
≥ 99%
Molecular Formula
C8H14NO3Cl
Molecular Weight
207.65
MDL Number
MFCD00190854
PubChem ID
306113
Melting Point
67-72 ºC
Appearance
White powder
Optical Rotation
[a]D20 = -16 ± 2º (C=2 in H2O)
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

Chloroacetyl-L-norleucine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceutical agents, particularly in the development of peptide-based drugs.
  • Biochemical Research: It is used to study enzyme activity and protein interactions, helping researchers understand biological processes at a molecular level.
  • Drug Design: The compound's unique structure allows it to act as a building block for designing new drugs, particularly those targeting specific receptors or enzymes.
  • Analytical Chemistry: Chloroacetyl-L-norleucine is employed in analytical methods to identify and quantify amino acids and peptides, enhancing the accuracy of biochemical assays.
  • Material Science: It can be incorporated into polymers to create materials with specific properties, such as improved thermal stability or enhanced mechanical strength.

Citations