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(4alpha,5alpha,17beta)-4,17-Dimethylspiro[androstane-3,3'-[3H]diazirin]-17-ol is a complex steroid derivative featuring a unique spiro-arrangement of androstane and a diazirin ring. This chemical compound is characterized by its specific structure, which includes a steroid backbone with additional methyl groups at the 4 and 17 positions. (4alpha,5alpha,17beta)-4,17-Dimethylspiro[androstane-3,3'-[3H]diazirin]-17-ol's intricate arrangement suggests potential biological activity and interactions with biological targets, making it a promising candidate for pharmaceutical or biochemistry research and development.

2398-56-3

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2398-56-3 Usage

Uses

Used in Pharmaceutical Research:
(4alpha,5alpha,17beta)-4,17-Dimethylspiro[androstane-3,3'-[3H]diazirin]-17-ol is used as a research compound for exploring its potential biological activity and interactions with various biological targets. (4alpha,5alpha,17beta)-4,17-Dimethylspiro[androstane-3,3'-[3H]diazirin]-17-ol's unique structure and steroidal backbone make it a valuable tool for investigating its pharmacological properties and possible therapeutic applications.
Used in Biochemical Studies:
In the field of biochemistry, (4alpha,5alpha,17beta)-4,17-Dimethylspiro[androstane-3,3'-[3H]diazirin]-17-ol serves as a key compound for understanding the interactions between steroid derivatives and biological systems. Its specific arrangement of the spiro and diazirin groups allows researchers to study the compound's effects on cellular processes and potential roles in various biological pathways.
Used in Drug Development:
(4alpha,5alpha,17beta)-4,17-Dimethylspiro[androstane-3,3'-[3H]diazirin]-17-ol is utilized as a starting point for the development of new drugs targeting specific biological processes. Its unique structure and potential pharmacological applications make it an attractive candidate for the creation of novel therapeutic agents, particularly in the areas of endocrinology and steroid-related disorders.
Used in Chemical Synthesis:
In the chemical synthesis industry, (4alpha,5alpha,17beta)-4,17-Dimethylspiro[androstane-3,3'-[3H]diazirin]-17-ol may be employed as a building block or intermediate for the creation of other complex steroidal compounds. Its unique structure can be further modified or functionalized to produce a variety of new molecules with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 2398-56-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2398-56:
(6*2)+(5*3)+(4*9)+(3*8)+(2*5)+(1*6)=103
103 % 10 = 3
So 2398-56-3 is a valid CAS Registry Number.

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