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1-Imidazolidinecarboxylic acid, 2-oxo-, also known as oxo-imidazolidine-4-carboxylate, is a chemical compound with the molecular formula C5H7NO3. It is a derivative of imidazolidinecarboxylic acid and plays a role in the biosynthesis of the amino acid histidine. 1-Imidazolidinecarboxylic acid, 2-oxois involved in the urea cycle, which is essential for the elimination of ammonia from the body. It is naturally found in protein-rich foods such as meat, fish, and dairy products. Due to its skin conditioning and antioxidant properties, 1-Imidazolidinecarboxylic acid, 2-oxohas potential applications in the pharmaceutical and cosmetic industries.

17607-02-2

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17607-02-2 Usage

Uses

Used in Pharmaceutical Industry:
1-Imidazolidinecarboxylic acid, 2-oxois used as an intermediate in the biosynthesis of histidine, an essential amino acid, for the development of pharmaceutical products.
Used in Cosmetic Industry:
1-Imidazolidinecarboxylic acid, 2-oxois used as a skin conditioning agent for its ability to improve skin texture and appearance.
Used in Antioxidant Formulations:
1-Imidazolidinecarboxylic acid, 2-oxois used as an antioxidant in cosmetic products to protect the skin from oxidative stress and environmental damage.

Check Digit Verification of cas no

The CAS Registry Mumber 17607-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,0 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17607-02:
(7*1)+(6*7)+(5*6)+(4*0)+(3*7)+(2*0)+(1*2)=102
102 % 10 = 2
So 17607-02-2 is a valid CAS Registry Number.

17607-02-2Relevant academic research and scientific papers

Solvent-accelerated decarboxylation of N-carboxy-2-imidazolidinone. Implications for stability of intermediates in biotin-dependent carboxylations

Rahil, Jubrail,You, Shaochun,Kluger, Ronald

, p. 12495 - 12498 (1996)

The decarboxylation of N-carboxy-2-imidazolidinone has previously been established as a model for the transfer of carbon dioxide from N(1')-carboxybiotin. The present paper reports the pH-dependence of the reaction as well as the acceleration of the reaction in methanol and in acetonitrile. These results suggest that enzymic reactions of N(1')-carboxybiotin in a hydrophobic active site with decreased hydrogen bonding can be rapid if the energy of desolvation is compensated by the energy made available by association of the substrate and protein. In addition, a report on the decarboxylation of N-carboxy-2-imidazolidinone in organic solvents containing macrocycles (Kluger, R.; Tsao, B.J. Am. Chem. Soc. 1993, 115, 2089-90) must be reinterpreted on the basis of the inherent instability of the substrate under the reaction conditions.

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