(5beta,9beta,10xi,15beta)-15-(acetyloxy)kaur-16-en-18-oic acid

Base Information

• Chemical Name: (5beta,9beta,10xi,15beta)-15-(acetyloxy)kaur-16-en-18-oic acid
• CAS No.: 6619-97-2
• Molecular Formula: C₂₂H₃₂O₄
• Molecular Weight: 360.494
• Mol file: 6619-97-2.mol

Synonyms:Xylopic saeure;15|A-Hydroxyprogesterone;

Chemical Property of (5beta,9beta,10xi,15beta)-15-(acetyloxy)kaur-16-en-18-oic acid

Chemical Property:

• Vapor Pressure: 2.46E-10mmHg at 25°C
• Boiling Point: 475.1°C at 760 mmHg
• Flash Point: 159°C
• PSA: 63.60000
• Density: 1.15g/cm³
• LogP: 4.58170

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: The compound "(5beta,9beta,10xi,15beta)-15-(acetyloxy)kaur-16-en-18-oic acid" has diverse applications across various fields. In the field of pharmacology and medicine, it may serve as a potential drug candidate or a precursor for the synthesis of pharmaceuticals due to its structural features and potential bioactive properties. In organic chemistry, it can be used as a starting material for the synthesis of various complex molecules, making it valuable for chemical research and drug development. Furthermore, in the field of natural product chemistry, this compound can be studied for its role in the biosynthesis of natural products and secondary metabolites in plants. Its versatility and potential pharmacological significance make it a valuable resource for researchers in these different fields.

Technology Process of (5beta,9beta,10xi,15beta)-15-(acetyloxy)kaur-16-en-18-oic acid

There total 2 articles about (5beta,9beta,10xi,15beta)-15-(acetyloxy)kaur-16-en-18-oic acid 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:

→ xylopic acid (6619-97-2,22343-40-4,73864-05-8)

Guidance literature:

aus 15β-Hydroxy-(-)-kaur-16-en-19-saeure u. Ac2O/Py;

Reference yield:

→ 15α-Acetoxy-Δ16-kauren-18α-saeure (6619-97-2,22343-40-4,73864-05-8)

Guidance literature:

aus Saeure II;

Reference yield: 86.0%

15β–acetoxy–(–)–kaur–16–en–l9–oic acid (6619-97-2) → 15-β-hydroxy-ent-kaur-16-en-19-oic acid (6619-95-0)

Guidance literature:

With potassium hydroxide; In methanol; for 6h; Reflux;

DOI:10.5935/0103-5053.20150287

Downstream raw materials:

grandifloric acid

15-β-hydroxy-ent-kaur-16-en-19-oic acid

methyl ent-15-oxokaur-16-en-19-oate

methyl ent-15α-hydroxykauran-19-oate