(S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid is a chemical compound with the molecular formula C5H8N2O3. It is an intermediate in the biosynthesis of the amino acid l-histidine, featuring a cyclic, five-membered structure with an imidazole ring and a carboxylic acid functional group. As a chiral molecule with a single chiral center, it exists in two enantiomers, (S)and (R)-. (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid holds potential in pharmaceutical and biochemical research due to its role as a precursor in l-histidine biosynthesis and its possible biological activities.
107716-98-3
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Basic information
- Product Name: (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid
- Synonyms: (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid
- CAS NO:107716-98-3
- Molecular Formula:
- Molecular Weight: 144.13
- EINECS: N/A
- Product Categories: N/A
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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: (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid(107716-98-3)
- EPA Substance Registry System: (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid(107716-98-3)
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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: 107716-98-3(Hazardous Substances Data)
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107716-98-3 Usage
Uses
Used in Pharmaceutical Research:(S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid is used as a key intermediate for the synthesis of l-histidine, which is an essential amino acid for various biological processes. Its role in the production of l-histidine makes it a valuable compound for pharmaceutical research and development.
Used in Biochemical Research:
In biochemical research, (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid serves as a precursor in the study of l-histidine biosynthesis. Understanding the biosynthetic pathways involving (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid can provide insights into the regulation of amino acid production and its implications in various biological systems.
Used in the Synthesis of Histidine Derivatives:
(S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid is used as a starting material for the synthesis of various histidine derivatives. These derivatives may have potential applications in the development of new drugs, as they can exhibit different biological activities compared to the parent compound.
Used in the Development of Chiral Molecules:
As a chiral molecule with two enantiomers, (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid is used in the development and study of chiral molecules. The different enantiomers can have distinct biological activities, making them important in the field of stereochemistry and drug design.
Used in the Study of Enzyme Mechanisms:
The role of (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid in the biosynthesis of l-histidine involves various enzymes. Studying the interactions between (S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid and the enzymes involved can provide valuable information on enzyme mechanisms and the regulation of metabolic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 107716-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,1 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.Calculate Digit Verification of CAS Registry Number 107716-98:
(8*1)+(7*0)+(6*7)+(5*7)+(4*1)+(3*6)+(2*9)+(1*8)=133
133 % 10 = 3
So 107716-98-3 is a valid CAS Registry Number.
107716-98-3Upstream product
107716-98-3Downstream Products
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(S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid
