34582-41-7 Usage
Uses
Used in Pharmaceutical Industry:
[(BENZYLAMINO)CARBONYL]AMINOACETIC ACID is used as a pharmaceutical compound for its ability to inhibit a specific enzyme involved in cancer cell growth. Its unique structure makes it a promising candidate for further research and development in drug discovery and design, potentially leading to the creation of novel treatments for various types of cancer.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [(BENZYLAMINO)CARBONYL]AMINOACETIC ACID serves as a valuable compound for studying its interactions with biological targets and understanding its potential therapeutic effects. This knowledge can be applied to the design of new drugs with improved efficacy and selectivity, ultimately contributing to advancements in medical treatments for cancer and other diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 34582-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,8 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34582-41:
(7*3)+(6*4)+(5*5)+(4*8)+(3*2)+(2*4)+(1*1)=117
117 % 10 = 7
So 34582-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O3/c13-9(14)7-12-10(15)11-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,13,14)(H2,11,12,15)
34582-41-7Relevant academic research and scientific papers
1-Carbamoylhydantoins. New Aspects of Reactivity
Kavina,Sizov
, p. 2119 - 2131 (2021/02/09)
Abstract: Some derivatives of 1-carbamoylhydantoins undergo cleavage at the N1–C(O) bond on heating in solution. 1-Carbamoylhydantoins in aqueous and alcoholic ammonia rearrange via opening of the imidazole ring, followed by recyclization. Prol
A facile synthesis of N-carbamoylamino acids
Bogolubsky, Andrey V.,Ryabukhin, Sergey V.,Pakhomov, Gennadiy G.,Ostapchuk, Eugeniy N.,Shivanyuk, Alexander N.,Tolmachev, Andrey A.
experimental part, p. 2279 - 2282 (2009/05/30)
N-Carbamoylamino acids were obtained through the alkylation of monosubstituted parabanic acids followed by hydrolysis of the intermediate products. This new methodology furnishes structurally and functionally diverse N-carbamoylamino acids in high preparative yields and excellent purity. Georg Thieme Verlag Stuttgart.
