Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a,7-dihydroxy-7-methyl-, methyl ester

Base Information

• Chemical Name: Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a,7-dihydroxy-7-methyl-, methyl ester
• CAS No.: 27934-98-1
• Deprecated CAS: 74688-55-4
• Molecular Formula: C17H26 O11
• Molecular Weight: 406.387

Synonyms:Tarphetalin;UNII-0L71794JC8;0L71794JC8;NSC 729640;Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a,7-dihydroxy-7-methyl-, methyl ester;27934-98-1

Chemical Property of Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a,7-dihydroxy-7-methyl-, methyl ester

Chemical Property:

• Vapor Pressure: 2.09E-19mmHg at 25°C
• Boiling Point: 645.8°C at 760 mmHg
• Flash Point: 230.9°C
• PSA: 175.37000
• Density: 1.58g/cm³
• LogP: -2.89180
• XLogP3: -2.2
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 5
• Exact Mass: 406.14751164
• Heavy Atom Count: 28
• Complexity: 639

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(CCC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O
• Isomeric SMILES: C[C@@]1(CC[C@]2([C@@H]1[C@@H](OC=C2C(=O)OC)OC3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O
• Uses: Ipolamiide is an extract from a plant which may display antiosteoporotic and antiinflammatory activity.

Technology Process of Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a,7-dihydroxy-7-methyl-, methyl ester

There total 13 articles about Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a,7-dihydroxy-7-methyl-, methyl ester 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:

8-epi-iridotrial glucoside (72963-55-4,80734-66-3) → ipolamiide (27934-98-1) + lamiide (27856-54-8)

Guidance literature:

In water; for 72h;

DOI:10.1016/S0031-9422(00)97538-1

Reference yield:

mussaenoside (64421-27-8,73284-85-2,149564-24-9) → ipolamiide (27934-98-1) + lamiide (27856-54-8)

Guidance literature:

In water; for 72h; Hebenstretia dentata;

DOI:10.1016/S0031-9422(00)97538-1

Reference yield:

C17H23(2)H3O9 (120481-59-6) → ipolamiide (27934-98-1) + lamiide (27856-54-8)

Guidance literature:

In water; for 72h; Hebenstretia dentata;

DOI:10.1016/S0031-9422(00)97538-1

upstream raw materials:

mussaenoside

C₁₇H₂₃⁽²⁾H₃O₉

8-epi-deoxyloganic acid

8-hydroxygeraniol

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