"14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy, acetate" is a complex organic compound belonging to the steroid family. It is characterized by a unique cyclic structure, with a 14,21-cyclo ring, and a pregnane core. The molecule features a 16.alpha.-carboxylic acid group, a 17-acetyl group, and a 3.beta.-hydroxy group, which are key functional groups that contribute to its chemical properties. 14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy-, acetate is further esterified with acetic acid, forming an acetate derivative. Such compounds are often studied for their potential biological activities and applications in the pharmaceutical industry, particularly in the development of drugs targeting hormonal systems.
7732-49-2
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Basic information
- Product Name: 14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy-, acetate
- Synonyms: 14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy-, acetate
- CAS NO:7732-49-2
- Molecular Formula:
- Molecular Weight: 0
- EINECS: N/A
- Product Categories: N/A
- Mol File: 7732-49-2.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy-, acetate(CAS DataBase Reference)
- NIST Chemistry Reference: 14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy-, acetate(7732-49-2)
- EPA Substance Registry System: 14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy-, acetate(7732-49-2)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 7732-49-2(Hazardous Substances Data)
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Chemical structure
A complex structure that includes a cyclopropyl ring, a carboxylic acid group, and an acetate group.Type of compound
A synthetic derivative of a steroid hormone.Potential pharmaceutical applications
The compound has potential pharmaceutical applications due to its steroidal nature.Derivative of
Progesterone, a naturally occurring hormone.Possible effects
The compound may have hormonal, anti-inflammatory, or other physiological effects.Further research and development
The specific properties and potential uses of the compound would depend on further research and development.Molecular weight
Approximately 398.54 g/mol (calculated from the chemical formula).Solubility
The compound's solubility in water or other solvents is not provided, but it is likely to be influenced by its steroidal structure and functional groups.Stability
The stability of the compound under various conditions (e.g., temperature, pH) is not provided, but it may be affected by the presence of the carboxylic acid and acetate groups.Synthesis
The compound is synthesized through chemical reactions involving the modification of the progesterone molecule.Purity
The purity of the compound would depend on the synthesis process and any subsequent purification steps.Stereoisomers
The compound may have stereoisomers due to the presence of chiral centers in the steroidal structure.Biological activity
The biological activity of the compound would depend on its interactions with specific receptors or enzymes in the body, which would require further investigation.Check Digit Verification of cas no
The CAS Registry Mumber 7732-49-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,3 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.Calculate Digit Verification of CAS Registry Number 7732-49:
(6*7)+(5*7)+(4*3)+(3*2)+(2*4)+(1*9)=112
112 % 10 = 2
So 7732-49-2 is a valid CAS Registry Number.
7732-49-2Upstream product
7732-49-2Downstream Products
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14,21-Cyclo-17.alpha.-pregna-5,20-diene-16.alpha.-carboxylic acid, 17-acetyl-3.beta.-hydroxy-, acetate
