211516-63-1 Usage
Description
Benzo[3,4]-18-norandrosta-3,5-diene-3(2'H)-carboxylic acid, 3',4',5',6'-tetrahydro-4',4',9,14-tetraMethyl-17-oxo-, Methyl ester, (3β,4β,8α,9β,10α,13α,14β)(9CI) is a complex steroidal chemical compound characterized by a unique molecular structure. It features a benzo ring, a carboxylic acid group, and a tetrahydro-4',4',9,14-tetramethyl-17-oxo moiety. Benzo[3,4]-18-norandrosta-3,5-diene-3(2'H)-carboxylic acid, 3',4',5',6'-tetrahydro-4',4',9,14-tetraMethyl-17-oxo-, Methyl ester, (3β,4β,8α,9β,10α,13α,14β)(9CI) exists in various stereoisomeric forms, as indicated by the 3β,4β,8α,9β,10α,13α,14β configuration. Benzo[3,4]-18-norandrosta-3,5-diene-3(2'H)-carboxylic acid, 3',4',5',6'-tetrahydro-4',4',9,14-tetraMethyl-17-oxo-, Methyl ester, (3β,4β,8α,9β,10α,13α,14β)(9CI) is of significant interest in pharmaceuticals and organic chemistry due to its potential biological activities and the possibility of synthesis and modification for a range of applications.
Uses
Used in Pharmaceutical Industry:
Benzo[3,4]-18-norandrosta-3,5-diene-3(2'H)-carboxylic acid, 3',4',5',6'-tetrahydro-4',4',9,14-tetraMethyl-17-oxo-, Methyl ester, (3β,4β,8α,9β,10α,13α,14β)(9CI) is used as a pharmaceutical intermediate for the development of drugs targeting various medical conditions. Its unique structure and potential biological activities make it a promising candidate for the synthesis of new therapeutic agents.
Used in Organic Chemistry Research:
In the field of organic chemistry, this compound serves as a valuable research tool for studying the synthesis and modification of steroidal compounds. Its complex structure and stereochemistry provide opportunities for exploring novel synthetic pathways and developing innovative methodologies for the preparation of related compounds.
Used in Drug Design and Development:
Benzo[3,4]-18-norandrosta-3,5-diene-3(2'H)-carboxylic acid, 3',4',5',6'-tetrahydro-4',4',9,14-tetraMethyl-17-oxo-, Methyl ester, (3β,4β,8α,9β,10α,13α,14β)(9CI)'s potential biological activities and structural features make it a candidate for drug design and development. It can be further modified and optimized to enhance its therapeutic properties, leading to the creation of new drugs with improved efficacy and selectivity.
Used in Steroid Hormone Analysis:
Due to its structural similarity to natural steroid hormones, Benzo[3,4]-18-norandrosta-3,5-diene-3(2'H)-carboxylic acid, 3',4',5',6'-tetrahydro-4',4',9,14-tetraMethyl-17-oxo-, Methyl ester, (3β,4β,8α,9β,10α,13α,14β)(9CI) can be employed as a reference compound in the analysis and identification of steroid hormones. This aids in understanding their roles in various physiological processes and the development of hormone-related therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 211516-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,5,1 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 211516-63:
(8*2)+(7*1)+(6*1)+(5*5)+(4*1)+(3*6)+(2*6)+(1*3)=91
91 % 10 = 1
So 211516-63-1 is a valid CAS Registry Number.