6949-60-6
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Basic information
- Product Name: N-formyl-4-nitro-phenylalanine
- Synonyms:
- CAS NO:6949-60-6
- Molecular Formula:
- Molecular Weight: 238.2
- EINECS: N/A
- Product Categories: N/A
- Mol File: 6949-60-6.mol
- Article Data: 0
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: N-formyl-4-nitro-phenylalanine(CAS DataBase Reference)
- NIST Chemistry Reference: N-formyl-4-nitro-phenylalanine(6949-60-6)
- EPA Substance Registry System: N-formyl-4-nitro-phenylalanine(6949-60-6)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 6949-60-6(Hazardous Substances Data)
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6949-60-6 Usage
Description
N-formyl-4-nitro-phenylalanine is a chemical compound derived from phenylalanine, an essential amino acid, with a nitro group and a formyl group attached to its aromatic ring. N-formyl-4-nitro-phenylalanine is characterized by its strong electron-withdrawing effect due to the nitro group and the added reactivity and functionality provided by the formyl group. These features make it a valuable tool in the study of peptide and protein structures and functions, as well as in various biochemical and biophysical research applications.Uses
Used in Research and Pharmaceutical Applications:N-formyl-4-nitro-phenylalanine is used as a research tool for studying the properties and behavior of amino acids and peptides in biological systems. Its unique structure allows for further modification and manipulation, making it a versatile compound for exploring the interactions and functions of peptides and proteins.
Used in Biochemical and Biophysical Studies:
The strong electron-withdrawing effect of the nitro group in N-formyl-4-nitro-phenylalanine makes it a useful compound for investigating the effects of electron-withdrawing groups on the structure and function of peptides and proteins. This can provide valuable insights into the role of such groups in biological systems and contribute to the development of new therapeutic strategies.
Used in the Study of Peptide and Protein Structures:
The formyl group in N-formyl-4-nitro-phenylalanine adds reactivity and functionality to the compound, enabling researchers to explore the structural aspects of peptides and proteins. This can lead to a better understanding of the factors that influence the folding, stability, and interactions of these biomolecules, which is crucial for the development of new drugs and therapies.
Used in the Investigation of Amino Acid Properties:
N-formyl-4-nitro-phenylalanine can be employed to study the properties of phenylalanine and other amino acids in various contexts. By examining how the presence of the nitro and formyl groups affects the behavior of the amino acid, researchers can gain a deeper understanding of the factors that influence the properties and functions of amino acids in biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 6949-60-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.Calculate Digit Verification of CAS Registry Number 6949-60:
(6*6)+(5*9)+(4*4)+(3*9)+(2*6)+(1*0)=136
136 % 10 = 6
So 6949-60-6 is a valid CAS Registry Number.
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6949-60-6Downstream Products
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N-formyl-4-nitro-phenylalanine
