5740-62-5 Usage
Uses
Used in Pharmaceutical Industry:
Prednicarbate Related Compound C (20 mg) (prednisolone-21-propionate) is used as an active pharmaceutical ingredient for the treatment of various inflammatory and immunological disorders. Its corticosteroid properties help in reducing inflammation, suppressing the immune system, and managing conditions such as allergies, asthma, and autoimmune diseases.
Used in Veterinary Medicine:
In the veterinary field, Prednicarbate Related Compound C (20 mg) (prednisolone-21-propionate) is used as a therapeutic agent for managing inflammation and immune-mediated conditions in animals. It can be prescribed for treating conditions like allergies, skin diseases, and respiratory issues in pets and livestock.
Used in Research and Development:
Prednicarbate Related Compound C (20 mg) (prednisolone-21-propionate) serves as a valuable compound in research and development for studying the effects of corticosteroids on various biological processes. It can be used in laboratory experiments to investigate the mechanisms of action, potential side effects, and interactions with other drugs or compounds.
Used in Drug Formulation:
Prednicarbate Related Compound C (20 mg) (prednisolone-21-propionate) is also utilized in the formulation of various pharmaceutical products, such as creams, ointments, and oral medications, targeting specific conditions that require localized or systemic corticosteroid treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 5740-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5740-62:
(6*5)+(5*7)+(4*4)+(3*0)+(2*6)+(1*2)=95
95 % 10 = 5
So 5740-62-5 is a valid CAS Registry Number.
5740-62-5Relevant academic research and scientific papers
Investigation on the Photostability of Halometasone and Prednicarbate in the Crystal State and Crystal Structure of Halometasone
Reisch, Johannes,Henkel, Gerald,Ekiz-Guecer, Nurten,Nolte, Gerald
, p. 63 - 68 (2007/10/02)
UV irradiation of halometasone (1) in the crystal state yields three photoproducts: 2-chloro-6α,9-difluoro-11β,17α-dihydroxy-16-α-methyl-3-oxoandrosta-1,4-diene-17β-carbaldehyde (3), 2-chloro-6α,9-difluoro-11β-hydroxy-16α-methylandrosta-1,4-diene-3,17-dione (4) and the dimerization product 2ξ-chloro-2ξ-(2-chloro-6α,9-difluoro-11β,21ξ-trihydroxy-16α-methyl-3,20-dioxopregna-1,4-dien-21-yl)-6α,9-difluoro-11β,17,21-trihydroxy-16α-methylpregna-4-ene-3,20-dione (5).The structure of 5 is determined by the molecular packing of 1 in the crystal, as shown by an X-ray analysis of 1.Two photoproducts are formed after irradiation of prednicarbate (2): 11β,17-dihydroxy-21-propionyloxypregna-1,4-diene-3,20-dione (6) and 17-(ethoxycarbonyloxy)-11β,21-dihydroxypregna-1,4-diene-3,20-dione (7). Key Words: Prednicarbate / Halometasone / Photochemistry
