2465-00-1

Basic information

• Product Name: acetate of cholest-7-en-3β-ol
• CAS NO: 2465-00-1
• Molecular Weight: 428.699
• Mol File: 2465-00-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: acetate of cholest-7-en-3β-ol(CAS DataBase Reference)
• NIST Chemistry Reference: acetate of cholest-7-en-3β-ol(2465-00-1)
• EPA Substance Registry System: acetate of cholest-7-en-3β-ol(2465-00-1)

Safety Data

• Hazardous Substances Data: 2465-00-1(Hazardous Substances Data)

Upstream product

• 80-99-9 lathosterol 
• 15459-85-5 5α-cholest-7-en-3-one 
• 566-27-8 cholest-5-en-3β,7β-diol 
• 809-51-8 7-ketocholesteryl acetate 
• 64110-39-0 C₃₇H₅₁N₃O₄ 
• 108-24-7 acetic anhydride 
• 6036-58-4 cholest-7-en-3β-ol 
• 6038-38-6 3β,7β-bis-benzoyloxy-cholest-5-ene 
• 434-16-2 7-dehydrocholesterol 
• 57-88-5 cholesterol 
• 40823-16-3 acetic acid-(7β-hydroxy-5α-cholestanyl-(3β)-ester) 
• 40823-41-4 acetic acid-(7α-hydroxy-5α-cholestanyl-(3β)-ester) 
• 71-23-8 propan-1-ol 
• 137637-33-3 5α-cholesta-6,8-dien-3β-ol 

Downstream Products

• 80-99-9 lathosterol 
• 6562-21-6 3β-(Acetyloxy)-5α-cholest-8(14)-ene 
• 15459-85-5 5α-cholest-7-en-3-one 
• 53755-39-8 (3S,5S,7S,8S,9R,10S,13R,14R,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopropa[7,8]cyclopenta[a]phenanthren-3-ol 
• 16780-48-6 3β-acetoxy-8α,14α-epoxy-5α-cholestan-7-one 
• 116561-41-2 3β-acetoxy-5α-cholest-8(14)-en-7-one-(p-toluene-sulfonylhydrazone) 
• 34495-42-6 3β-acetoxy-5α-cholest-8(14)-en-15-one 
• 566-99-4 5α-cholest-8(14)-en-3β-ol 
• 69140-06-3 5α-cholest-8(14)-ene-3β,7α-diol 
• 34227-11-7 3β-hydroxy-5α-cholesta-7,14-diene 
• 50673-97-7 15-Ketocholestene 
• 566-29-0 3β-hydroxy-5α-cholest-8(14)-en-7-one 
• 69140-15-4 3β-hydroxy-5α-cholest-8-en-7-one 
• 2665-03-4 [choleste-7-ene-3-oxy]trimethylsilane 

Relevant articles and documents

A Simple Method for the Reduction of the 7,8-Double Bond of Steroidal 5,7-Dienes

1,4-Cycloadducts of various steroidal 5,7-dienes and 4-phenyl-1,2,4-triazoline-3,5-dione gave a separable mixture (3 : 2) of the corresponding Δ5- and Δ7-sterols in good yield when treated with lithium dissolved in refluxing ethylamine.

Preparation of steroid olefins from heptafluorobutyrates

Steroids with hydroxyl group in positions 2, 3, 6, 7, 17 and 20 were esterified with heptafluorobutyric anhydride. The obtained esters on treatment with lithium bromide in N,N-dimethylacetamide in the presence of pyridinium tosylate afforded the corresponding olefins in high yields.

Studies on the Constituents of Pollen. X. On the Constituents of Pollen Grains of Ambrosia elatior LINNE

The new sterols 4α,14-dimethyl-9,19-cyclocholestan-3β,24ξ-diol (IIIa) and 4α,14-dimethyl-9,19-cyclocholestan-3β,24ξ,25-triol (IVa) were isolated, together with lophenone, lophenol, and cholest-7-en-3β-ol, from the pollen grains of Ambrosia elatior LINNE.The structures were elucidated on the basis of spectroscopic studies and chemical evidence.Keywords-Ambrosia elatior LINNE; Compositae; pollen grains; lophenone; lophenol; cholest-7-en-3β-ol; 4α,14-dimethyl-9,19-cyclocholestan-3β,24ξ-diol; 4α,14-dimethyl-9,19-cyclocholestan-3β,24ξ,25-triol