4885-81-8 Usage
Uses
Used in Pharmaceutical Industry:
D-(-)-α-(m-nitrophenyl)glycine is used as a key intermediate in the synthesis of pharmaceuticals for the treatment of cancer. Its ability to inhibit the activity of enzymes involved in tumor growth makes it a valuable component in the development of anticancer drugs.
Used in Research and Development:
D-(-)-α-(m-nitrophenyl)glycine serves as a crucial tool in the research and development of new drugs, particularly those targeting cancer. Its unique structure and functionality allow scientists to explore its potential in the synthesis of other biologically active compounds, further expanding its applications in medicinal chemistry and drug discovery.
Used in Drug Synthesis:
D-(-)-α-(m-nitrophenyl)glycine is used as a building block in the synthesis of various biologically active compounds. Its chiral nature and the presence of a nitrophenyl group make it an ideal candidate for the development of novel pharmaceuticals with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4885-81-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4885-81:
(6*4)+(5*8)+(4*8)+(3*5)+(2*8)+(1*1)=128
128 % 10 = 8
So 4885-81-8 is a valid CAS Registry Number.
4885-81-8Relevant academic research and scientific papers
D-phenyl glycine derivative and its preparation and use
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Paragraph 0051-0052, (2016/12/01)
The invention discloses D-phenylglycine derivatives as shown in a formula I. In the formula 1, XR2 is methoxy, and R1 is ethyl, (N-fmoc-amino) methyl and the like; or R1 is chloromethyl, and XR2 is ethoxy, butoxy, N-(2-hydroxyethyl) amino, N-methylamino,
The reaction of optically active α-aminocarboxylic acid hydrazides with triethyl orthoesters
Kudelko, Agnieszka,Zieliński, Wojciech,Ejsmont, Krzysztof
experimental part, p. 7838 - 7845 (2011/10/12)
New derivatives of 2-(1-amino-1-phenylmethyl)-1,3,4-oxadiazole and 1,2,4-triazin-6-one were synthesised in the reactions of optically active α-aminocarboxylic acid hydrazides and triethyl orthoesters in xylene. The electronic and steric effects of substituents at the α position influencing the formation of five- or six-membered products are discussed.
