Liriope muscari baily saponins C

Base Information

• Chemical Name: Liriope muscari baily saponins C
• CAS No.: 87480-46-4
• Molecular Formula: C₄₄H₇₀O₁₆
• Molecular Weight: 855.03
• Hs Code.: 29389090
• Mol file: 87480-46-4.mol

Synonyms:Ruscogenin-1-O-[b-D-glucopyranosyl(1→2)][b-D-xylopyranosyl (1→3)]-b-D-fucopyranoside;

Chemical Property of Liriope muscari baily saponins C

Chemical Property:

• PKA: 12.78±0.70(Predicted)
• PSA: 235.68000
• Density: 1.40
• LogP: 0.85320
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C

Purity/Quality:

98%,99%, ^*data from raw suppliers

Liriope muscari baily saponins C ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Liriope Muscari Baily Saponins C is a naturally occurring steroidal sapogenin and saponin derivative.

Technology Process of Liriope muscari baily saponins C

There total 1 articles about Liriope muscari baily saponins C which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ Ophiopogonin D' (65604-80-0,87480-46-4,143051-93-8,146388-18-3)

Guidance literature:

Ophiopogonin B' (IV), 0.5percentKOH-Aethanol;

Reference yield:

mixture of 3-O-<α-L-rhamnopyranosyl-(1->2)><β-D-xylopyranosyl(1->3)>-β-D-glucopyranosides of diosgenin and yamogenin (65604-80-0,87480-46-4,143051-93-8,146388-18-3) → glucosazone (534-97-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 2 N HCl-50 percent dioxane / 3 h / Heating

2: AcONa / H₂O / 0.5 h / Heating

With hydrogenchloride; sodium acetate; In water;

Reference yield:

acetic anhydride (108-24-7) + mixture of 3-O-<α-L-rhamnopyranosyl-(1->2)><β-D-xylopyranosyl(1->3)>-β-D-glucopyranosides of diosgenin and yamogenin (65604-80-0,87480-46-4,143051-93-8,146388-18-3) → D-Xylose (87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2) + Diosgenin monoacetate (1061-54-7,1180-12-7,33282-86-9,41336-81-6,75246-99-0,122405-26-9,122405-31-6) + yamogenin-acetate (1061-54-7,1180-12-7,33282-86-9,41336-81-6,75246-99-0,122405-26-9,122405-31-6) + L-rhamnose (73-34-7)

Guidance literature:

With pyridine; hydrogenchloride; Multistep reaction. Further byproducts given; 1.) reflux, 3 h;

Downstream raw materials:

D-Xylose

Diosgenin monoacetate

yamogenin-acetate

L-rhamnose