28416-84-4 Usage
Description
(6a,11b,16a,17a)-6,9-Difluoro-11,17-dihydroxy-16-methyl-3-oxoandrosta-1,4-diene-17-carboxylic acid methyl ester is a steroid derivative with the molecular formula C23H29F2O4. It is a synthetic compound characterized by the presence of two fluorine atoms, two hydroxyl groups, a carboxylic acid functional group, and a methyl ester moiety. Due to its structural similarities to natural steroids, this compound holds potential for various applications in the pharmaceutical industry, although further research is necessary to fully comprehend its therapeutic capabilities.
Uses
Used in Pharmaceutical Research:
(6a,11b,16a,17a)-6,9-Difluoro-11,17-dihydroxy-16-methyl-3-oxoandrosta-1,4-diene-17-carboxylic acid methyl ester is used as a research compound for exploring its potential applications in the treatment of various medical conditions. Its structural resemblance to natural steroids suggests that it may have therapeutic properties that could be harnessed for drug development.
Used in Drug Development:
In the pharmaceutical industry, (6a,11b,16a,17a)-6,9-Difluoro-11,17-dihydroxy-16-methyl-3-oxoandrosta-1,4-diene-17-carboxylic acid methyl ester is utilized as a starting material or a key intermediate in the synthesis of novel steroidal drugs. Its unique functional groups and fluorinated nature may offer advantages in terms of pharmacokinetics, selectivity, and potency compared to non-fluorinated steroidal compounds.
Used in Medical Treatments:
Although further research is required, (6a,11b,16a,17a)-6,9-Difluoro-11,17-dihydroxy-16-methyl-3-oxoandrosta-1,4-diene-17-carboxylic acid methyl ester may eventually be used as an active pharmaceutical ingredient in the treatment of specific medical conditions. Its potential applications could include hormone-related disorders, inflammatory conditions, or other diseases where steroidal compounds have demonstrated therapeutic benefits.
Used in Chemical Synthesis:
(6a,11b,16a,17a)-6,9-Difluoro-11,17-dihydroxy-16-methyl-3-oxoandrosta-1,4-diene-17-carboxylic acid methyl ester serves as a versatile building block in the synthesis of other complex organic molecules, particularly those with steroidal frameworks. Its unique functional groups and fluorine atoms can be exploited in various synthetic routes to access a diverse range of steroidal compounds with tailored properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 28416-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,1 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28416-84:
(7*2)+(6*8)+(5*4)+(4*1)+(3*6)+(2*8)+(1*4)=124
124 % 10 = 4
So 28416-84-4 is a valid CAS Registry Number.
