5407-25-0 Usage
Uses
Used in Organic Synthesis:
AMINO-(4-NITRO-PHENYL)-ACETIC ACID is utilized as a key intermediate in the synthesis of various organic compounds. Its presence of both amino and nitro groups allows for versatile chemical reactions, making it a valuable building block in the creation of new molecules with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, AMINO-(4-NITRO-PHENYL)-ACETIC ACID is employed as a starting material for the development of new drugs and pharmaceuticals. Its structural features and potential biological activities make it a promising candidate for the discovery of novel therapeutic agents.
Used in Drug Development:
Due to its potential biological activities, AMINO-(4-NITRO-PHENYL)-ACETIC ACID may be used in the development of new drugs targeting specific diseases or conditions. Its unique structure can be modified to create derivatives with enhanced pharmacological properties, contributing to the advancement of medicine.
It is crucial to handle AMINO-(4-NITRO-PHENYL)-ACETIC ACID with care, as it may pose risks to human health and the environment if not properly managed and disposed of. Proper safety measures and disposal protocols should be followed to minimize any potential hazards associated with AMINO-(4-NITRO-PHENYL)-ACETIC ACID.
Check Digit Verification of cas no
The CAS Registry Mumber 5407-25-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5407-25:
(6*5)+(5*4)+(4*0)+(3*7)+(2*2)+(1*5)=80
80 % 10 = 0
So 5407-25-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O4/c9-7(8(11)12)5-1-3-6(4-2-5)10(13)14/h1-4,7H,9H2,(H,11,12)
5407-25-0Relevant academic research and scientific papers
Preparation method for D, L-phenylglycine and analogue thereof
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Paragraph 0053; 0054, (2017/03/17)
The invention provides a preparation method for D, L-phenylglycine and an analogue thereof. According to the method, benzaldehyde, an analogue thereof and hydrocyanic acid are adopted as raw materials and subjected to cyanidation reaction, and then 2-hydroxy-benzyl cyanide or 2-hydroxy-benzyl cyanide analogue (cyanohydrin for short) is generated. Cyanohydrin reacts with carbon dioxide and the aqueous solution of ammonia, and then 5-phenyl-hydantoin and an analogue thereof (hydantoin for short) are generated. hydantoin is successively subjected to steam stripping, alkaline hydrolysis, steam stripping, decolorization, neutralization, crystallization, washing, centrifuging, drying and the like to obtain D, L-phenylglycine and the analogue thereof. Compared with the prior art, the preparation method for D, L-phenylglycine and the analogue thereof can significantly and effectively reduce the pollution, and fewer inorganic salt by-products are generated. Meanwhile, the prepared D, L-phenylglycine and the analogue thereof are high in product yield and high in purity. Counted in benzaldehyde and the analogue thereof, the yield of D, L-phenylglycine and the analogue thereof is larger than or equal to 96%, and the product purity is larger than or equal to 99%. Meanwhile, the process flow is simple and feasible, so that the method is worthy of market popularization and application.
