6155-50-6

Basic information

• Product Name: (1beta,3beta,22xi)-spirost-5-en-1,3-diyl diacetate
• CAS NO: 6155-50-6
• Molecular Formula: C₃₁H₄₆O₆
• Molecular Weight: 514.6933
• Mol File: 6155-50-6.mol

Chemical Properties

• Boiling Point: 577.3°C at 760 mmHg
• Flash Point: 241.2°C
• Density: 1.16g/cm³
• Vapor Pressure: 2.52E-13mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: (1beta,3beta,22xi)-spirost-5-en-1,3-diyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (1beta,3beta,22xi)-spirost-5-en-1,3-diyl diacetate(6155-50-6)
• EPA Substance Registry System: (1beta,3beta,22xi)-spirost-5-en-1,3-diyl diacetate(6155-50-6)

Safety Data

• Hazardous Substances Data: 6155-50-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(1beta,3beta,22xi)-Spirost-5-en-1,3-diyl diacetate is used as a pharmaceutical precursor for the development and synthesis of new drugs. Its steroid nature makes it a promising candidate for creating compounds that can target specific biological pathways or receptors, potentially leading to the discovery of novel therapeutic agents.
Used in Drug Development:
(1beta,3beta,22xi)-Spirost-5-en-1,3-diyl diacetate is utilized in drug development as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of new molecules with potential therapeutic properties, contributing to the advancement of medicine and healthcare.
It is important to handle (1beta,3beta,22xi)-spirost-5-en-1,3-diyl diacetate with care, as it may have certain hazards associated with its handling and use. Proper safety measures should be taken to minimize any risks during its application in research and development.

Upstream product

• 108-24-7 acetic anhydride 
• 472-11-7 (25R)-ruscogenin 
• 472-11-7 25(S)-ruscogenin 
• 38971-41-4 25(S)-ruscogenin 1-O-α-L-rhamnopyranosyl-(1->2)-β-D-fucopyranoside 
• 87425-34-1 25(S)-ruscogenin 1-O-β-D-fucopyranosido-3-O-α-L-rhamnopyranoside 
• 87436-70-2 25(S)-ruscogenin 3-O-L-rhamnopyranoside 
• 472-11-7 25(S)-ruscogenin 
• 105798-62-7 alliofuroside A 
• 105822-00-2 22-O-methyl ether of alliofuroside A 
• 39491-38-8 alliospiroside A 

Relevant articles and documents

STEROIDS OF THE SPIROSTAN AND FUROSTAN SERIES FROM PLANTS OF THE GENUS Allium. XXI. STRUCTURE OF ALLIOSPIROSIDE A AND ALLIOFUROSIDE A FROM Allium cepa

Two new steroid glycosides have been isolated from the generative organs (pericarps and peduncles) of Allium cepa L.: alliospiroside A and alliofuroside A.According to chemical transformations and spectral characteristics, alliospiroside A has the structure of (25S)-spirost-5-ene-1β,3β-diol 1-O- 2)-α-L-arabinopyranoside>.The structure of (25S)-furost-5-ene-1β,3β,22α,26-tetraol 20-O-β-D-glucopyranoside 1-O- 2)-α-L-arabinopyranoside> has been established for alliofuroside A.

Comparative Studies on the Constituents of Ophiopogonis Tuber and Its Congeners. I. Studies of the Constituents of the Subterranean Part of Liriope platyphylla Wang et Tang.

Eight steroidal glycosides, tentatively named glycosides A(1), B(2), C(3), D(4), E(5), F(6), G(7) and H(8), were isolated from the methanol extract of the subterranean part of Liriope platyphylla Wang et Tang (Liliaceae).The structures of these glycosides were established as ruscogenin 3-O-α-L-rhamnopyranoside (1), 25(S)-ruscogenin 1-O-β-D-fucopyranosido-3-O-α-L-rhamnopyranoside (2), 25(S)-ruscogenin 1-O-α-L-rhamnopyranosyl-(1->2)-β-D-fucopyranoside (3), ruscogenin 3-O-β-D-glucopyranosyl(1->3)-α-L-rhamnopyranoside (4), a mixture of 3-O-2)>3)>-β-D-glucopyranosides of diosgenin and yamogenin (=a mixture of ophiopogonin D' and its 25(S)-isomer, 5), a mixture of 3-O-β-chacotriosides of diosgenin and yamogenin (= a mixture of dioscin and its 25(S)-isomer, 6), ruscogenin 1-sulfate 3-O-α-L-rhamnopyranoside (7), and 26-O-β-D-glucopyranosyl-22-O-methylfurost-5-ene-3β,26-diol 3-O-β-chacotrioside (=methyl proto-dioscin, 8).