25615-11-6

Basic information

• Product Name: 17BETA(H),21BETA(H)-HOP-22(29)-EN-3-ONE
• Synonyms: 17BETA(H),21BETA(H)-HOP-22(29)-EN-3-ONE;17(H),21(H)-Hop-22(29)-en-3-one
• CAS NO: 25615-11-6
• Molecular Formula: C30H48O
• Molecular Weight: 424.708
• Mol File: 25615-11-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 485.7±14.0 °C(Predicted)
• Appearance: /
• Density: 0.973±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 17BETA(H),21BETA(H)-HOP-22(29)-EN-3-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 17BETA(H),21BETA(H)-HOP-22(29)-EN-3-ONE(25615-11-6)
• EPA Substance Registry System: 17BETA(H),21BETA(H)-HOP-22(29)-EN-3-ONE(25615-11-6)

Safety Data

• Hazardous Substances Data: 25615-11-6(Hazardous Substances Data)

Usage

Class

Organic compounds

Subclass

Estrogens and derivatives

Type

Steroid

Natural occurrence

Found in animals

Involvement

Biosynthesis of steroids and steroid hormones

Usage

Production of pharmaceuticals and hormones

Chemical structure

Cyclopentanophenanthrene backbone and a beta-hydroxyketone group

Biological activity

Exhibits hormone-like effects in the body

Potential applications

Treatment of hormone-related conditions and diseases
It's worth noting that the compound is a steroid, which is a type of organic compound that has a specific structure and is involved in the biosynthesis of other steroids and steroid hormones. The compound is also used in the production of pharmaceuticals and hormones, which suggests that it has potential therapeutic uses. The chemical structure of the compound consists of a cyclopentanophenanthrene backbone and a beta-hydroxyketone group, which may be responsible for its hormone-like effects in the body. Studies have shown that the compound has potential applications in the treatment of hormone-related conditions and diseases, which further highlights its potential therapeutic uses.

Upstream product

• 1981-81-3 hydroxyhopanone 
• 58801-23-3 3β-hydroxy-hop-22(29)-ene 

Downstream Products

• 17152-56-6 hopenone a 
• 1615-91-4 diploptene 
• 1177-74-8 (3S,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3-Acetyl-5a,5b,8,8,11a,13b-hexamethyl-icosahydro-cyclopenta[a]chrysen-9-one 
• 1812-61-9 (3S,3aS,5aR,5bR,11aR,13aR,13bS)-3-Isopropyl-5a,5b,8,8,11a,13b-hexamethyl-icosahydro-cyclopenta[a]chrysen-9-ol 
• 1678-31-5 moretenol 
• 58801-23-3 3β-hydroxy-hop-22(29)-ene 
• 28196-47-6 hydroxyhopane 
• 60686-85-3 21αH-29-nor-hopan-3,28-dion 
• 2085-25-8 Acetic acid (3R,3aS,5aR,5bR,11aR,13aR,13bS)-3-isopropenyl-5a,5b,8,8,11a,13b-hexamethyl-icosahydro-cyclopenta[a]chrysen-9-yl ester 

Relevant articles and documents

HOPENOL-B, A TRITERPENE ALCOHOL FROM EUPHORBIA SUPINA

In addition to the known triterpene motiol, hopenol-b (hop-22(29)-en-3β-ol) was isolated from the whole herb of Euphorbia supina.It has not been found previously in nature, though it has been prepared by both synthetic and biosynthetic methods. Key Word Index - Euphorbia supina; Euphorbiaceae; triterpenes; motiol; hopenol-b.

Partial synthesis of dihydrothysanolactone

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