36623-16-2Relevant articles and documents
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Huang-Minlon et al.
, p. 5394 (1952)
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36623-16-2
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Basic information
- Product Name: 5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE
- Synonyms: 5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE;UROCORTISONE 3-ACETATE;(3alpha,5beta)-3-(Acetyloxy)-17,21-dihydroxy-pregnane-11,20-dione
- CAS NO:36623-16-2
- Molecular Formula: C23H34O6
- Molecular Weight: 406.51
- EINECS: N/A
- Product Categories: N/A
- Mol File: 36623-16-2.mol
- Article Data: 1
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 547.5±50.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.24±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 12.36±0.70(Predicted)
- CAS DataBase Reference: 5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE(CAS DataBase Reference)
- NIST Chemistry Reference: 5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE(36623-16-2)
- EPA Substance Registry System: 5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE(36623-16-2)
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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: 36623-16-2(Hazardous Substances Data)
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36623-16-2 Usage
Description
5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE is a steroidal compound derived from the pregnane family, characterized by its unique molecular structure featuring three hydroxyl groups and two ketone groups. It is known for its potential applications in various fields due to its distinct chemical properties.Uses
Used in Pharmaceutical Industry:5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE is used as an intermediate compound for the synthesis of various steroidal drugs. Its unique structure allows for the development of medications targeting hormonal imbalances and other related health issues.
Used in Immunoassay Development:
In the field of immunoassays, 5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE serves as a key component in the synthesis of carboxylated derivatives of tetrahydrocortisol and tetrahydrocortisone. These derivatives are essential for creating specific and sensitive immunoassays, which are crucial diagnostic tools in the detection and measurement of various steroidal hormones in biological samples.
Check Digit Verification of cas no
The CAS Registry Mumber 36623-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.Calculate Digit Verification of CAS Registry Number 36623-16:
(7*3)+(6*6)+(5*6)+(4*2)+(3*3)+(2*1)+(1*6)=112
112 % 10 = 2
So 36623-16-2 is a valid CAS Registry Number.
36623-16-2Upstream product
- 115586-86-2 3α,17,21-triacetoxy-5β-pregnane-11,20-dione
- 83274-79-7 3α-acetoxy-17α,21-dihydroxy-5β-pregnane-11,20-dione 21-tert-butyldimethylsilyl ether
- 50-03-3 hydrocortisone acetate
- 1482-50-4 5β-pregnane-11β,17α,21-triol-3,20-dione
- 64313-94-6 RU 18760
- 79489-01-3 tetrahydrocortisol 21-tert-butildimethylsilyl ether
- 28439-40-9 3α,21-diacetoxy-17-hydroxy-5β-pregnane-11,20-dione
- 83274-78-6 3α-acetoxy-11β,17α,21-trihydroxy-5β-pregnan-20-one 21-tert-butyldimethylsilyl ether
- 79489-00-2 5β-dihydrocortisol 21-tert-butyldimethylsilyl ether
36623-16-2Downstream Products
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5-BETA-PREGNAN-3-ALPHA, 17,21-TRIOL-11,20-DIONE 3-ACETATE
