73629-43-3 Usage
Uses
Used in Pharmaceutical Industry:
Benzonitrile, 2,3-diaminois used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a versatile building block for the development of new drugs.
Used in Dye Industry:
Benzonitrile, 2,3-diaminois used in the production of dyes due to its ability to form colored compounds. Its chemical properties make it suitable for creating a wide range of colors.
Used in Organic Compounds Synthesis:
Benzonitrile, 2,3-diaminois used as a building block in the synthesis of various organic compounds. Its unique structure allows for the creation of a diverse range of chemical products.
Used in Antimicrobial Applications:
Benzonitrile, 2,3-diaminois used as a potential candidate for the development of new antimicrobial agents due to its antibacterial and antifungal properties. Its ability to inhibit the growth of harmful microorganisms makes it a promising compound for use in this field.
Used in Material Development:
Benzonitrile, 2,3-diaminois being investigated for its potential use in the development of new materials, such as polymers and coatings. Its unique chemical properties make it a valuable component in the creation of innovative materials with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 73629-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73629-43:
(7*7)+(6*3)+(5*6)+(4*2)+(3*9)+(2*4)+(1*3)=143
143 % 10 = 3
So 73629-43-3 is a valid CAS Registry Number.
73629-43-3Relevant academic research and scientific papers
COMPOUNS, COMPOSITIONS AND METHODS OF USE
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, (2018/07/29)
Herein, compounds, compositions and methods for modulating inclusion formation and stress granules in cells related to the onset of neurodegenerative diseases, musculoskeletal diseases, cancer, ophthalmological diseases, and viral infections are described.
Synthesis and potent antifungal activity against Candida species of some novel 1H-benzimidazoles
Goeker, Hakan,Alp, Mehmet,Ates-Alagoez, Zeynep,Yildiz, Sulhiye
experimental part, p. 936 - 948 (2009/12/05)
(Chemical Equation Presented) A series of 47 novel N1-alkylated- 2-aryl-5(6)-substituted-1H-benzimidazoles and their three novel indole analogues were synthesized and evaluated for in vitro antifungal activities against Candida species by the tube dilution method. The results showed that compounds 79 and 80, having pyridine at the position C-2, of benzimidazoles exhibited the greatest activity with MIC values of 6.25-3.12 μg/mL. Indole analogues 108-110 have no inhibitory activity.
