Mammoside I

Base Information

• Chemical Name: Mammoside I
• CAS No.: 126642-32-8
• Molecular Formula: C40H72 O19
• Molecular Weight: 857
• Mol file: 126642-32-8.mol

Synonyms:Hexadecanoicacid, 11-[(O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-6-deoxy-b-D-galactopyranosyl)oxy]-,(S)-; Mammoside I; Operculinic acid C

Chemical Property of Mammoside I

Chemical Property:

• Boiling Point: 977.7±65.0 °C(Predicted)
• PKA: 4.78±0.10(Predicted)
• PSA: 293.21000
• Density: 1.35±0.1 g/cm3(Predicted)
• LogP: -0.06970

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Mammoside I

There total 9 articles about Mammoside I 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:

(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(3-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,2''-ester (1255952-64-7) → lauric acid (143-07-7) + 1-decanoic acid (334-48-5) + (E)-3-phenylacrylic acid (140-10-3) + (11S)-hydroxyhexadecanoic acid 11-O-α-L-rhamnopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→2)-O-β-D-fucopyranoside (126642-32-8)

Guidance literature:

With water; potassium hydroxide; In methanol; at 90 ℃; for 2h;

DOI:10.1021/np100283t

Reference yield:

(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester (1255952-66-9) → lauric acid (143-07-7) + 1-decanoic acid (334-48-5) + (E)-3-phenylacrylic acid (140-10-3) + (11S)-hydroxyhexadecanoic acid 11-O-α-L-rhamnopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→2)-O-β-D-fucopyranoside (126642-32-8)

Guidance literature:

With water; potassium hydroxide; In methanol; at 90 ℃; for 2h;

DOI:10.1021/np100283t

Reference yield:

(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(3-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester (1255952-67-0) → lauric acid (143-07-7) + 1-decanoic acid (334-48-5) + (E)-3-phenylacrylic acid (140-10-3) + (11S)-hydroxyhexadecanoic acid 11-O-α-L-rhamnopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→2)-O-β-D-fucopyranoside (126642-32-8)

Guidance literature:

With water; potassium hydroxide; In methanol; at 90 ℃; for 2h;

DOI:10.1021/np100283t

upstream raw materials:

diazomethane

(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(3-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,2''-ester

(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-dodecanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,2''-ester

(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester

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