10133-85-4 Usage
Uses
Used in Pharmaceutical Industry:
(5-AMINO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID is used as a potential building block for the synthesis of other compounds due to its unique structure and functional groups. Its presence of an amino group and a carboxylic acid group may allow it to form various interactions with biological targets, making it a candidate for the development of new pharmaceutical agents.
Used in Drug Discovery and Development:
In the Drug Discovery and Development sector, (5-AMINO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID is used as a starting material for the synthesis of novel compounds with potential therapeutic properties. Its ability to interact with biological targets could lead to the discovery of new drugs with improved efficacy and selectivity.
Used in Medicinal Chemistry Research:
(5-AMINO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID is utilized in medicinal chemistry research to investigate its potential as a therapeutic agent. Its structure and functional groups may provide insights into the design of new drugs with specific biological activities, contributing to the advancement of medicinal chemistry.
Note: Since the provided materials do not specify particular applications or industries for (5-AMINO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID, the uses listed above are inferred based on its potential properties and the general applications of similar compounds in the pharmaceutical and chemical research fields. Further investigation and research would be necessary to confirm these uses and identify additional applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10133-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10133-85:
(7*1)+(6*0)+(5*1)+(4*3)+(3*3)+(2*8)+(1*5)=54
54 % 10 = 4
So 10133-85-4 is a valid CAS Registry Number.
10133-85-4Relevant academic research and scientific papers
Li, Jian
, p. 428 - 431 (2010)
The compound N-(N-acetic acid-yl-phthalimide-5-yl) maleamic acid (C 14H10N2O7, M r = 318) was synthesized and its structure was characterized by elemental analysis, 1H NMR and IR spectra. The single crystal of the title compound (C14H14N2O9, M r = 354.27) was cultured and its structure was determined by single crystal X-ray diffraction. The crystal belongs to monoclinic system, space group P21/c with a = 14.3859(19), b = 12.5835(18), c = 8.6934(15) A, β = 102.824(2)°, V = 1534.5(4) A3, Z = 4, D c = 1.534 g cm-3, μ(Mo Kα) = 0.131 mm-1, F(000) = 736. The final refinement gave R = 0.0652, wR(F 2) = 0.1239 for 2,703 observed reflections with I > 2σ(I). X-ray diffraction analysis reveals that the asymmetric unit of the title compound contains one N-(N-acetic acid-yl-phthalimide-5-yl) maleamic acid molecule and two water molecules. One of the two water molecules is disordered. The phthalimide group is essentially planar. The crystal structure of the title compound is stabilized by N-H...O and O-H...O hydrogen bonds interactions. The compound N-(N-acetic acid-yl-phthalimide-5-yl) maleamic acid possesses moderate antibacterial activity.
