Phenylethyl primeveroside

Base Information

• Chemical Name: Phenylethyl primeveroside
• CAS No.: 129932-48-5
• Molecular Formula: C19H28 O10
• Molecular Weight: 416.425
• Wikidata: Q105381978
• Mol file: 129932-48-5.mol

Synonyms:Phenylethyl primeveroside;Compound NP-001284;CHEBI:167926;AKOS040740070;NCGC00380502-01;2-(2-phenylethoxy)-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol;NCGC00380502-01_C19H28O10_beta-D-Glucopyranoside, 2-phenylethyl 6-O-beta-D-xylopyranosyl-

Chemical Property of Phenylethyl primeveroside

Chemical Property:

• Vapor Pressure: 2.18E-18mmHg at 25°C
• Boiling Point: 661.3°Cat760mmHg
• PKA: 12.89±0.70(Predicted)
• Flash Point: 353.7°C
• PSA: 158.30000
• Density: 1.49g/cm³
• LogP: -2.49110
• XLogP3: -2.2
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 7
• Exact Mass: 416.16824709
• Heavy Atom Count: 29
• Complexity: 488

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O

Technology Process of Phenylethyl primeveroside

There total 18 articles about Phenylethyl primeveroside 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: 77.0%

2-phenylethyl 2,3,4,2',3',4'-hexa-O-benzoyl-β-primeveroside (192827-13-7) → 2-phenylethyl β-primeveroside (129932-48-5)

Guidance literature:

With sodium methylate; In methanol; at 20 ℃; for 12h;

DOI:10.1271/bbb.65.2719

Reference yield: 70.0%

phenethyl 2,3,4,2',3',4'-O-hexaacetyl-β-D-xylopyranosyl-(1->6)-β-D-glucopyranoside (132278-39-8) → 2-phenylethyl β-primeveroside (129932-48-5)

Guidance literature:

With potassium carbonate; In methanol; at 20 ℃; for 0.5h;

DOI:10.3987/COM-05-10383

Reference yield: 70.0%

2-phenylethanol (60-12-8) + p-nitrophenyl 6-O-β-D-xylopyranosyl-β-D-glucopyranoside → 2-phenylethyl β-primeveroside (129932-48-5)

Guidance literature:

With sodium acetate buffer; Penicillium multicolor IAM7153 β-primeverosidase; In water; at 40 ℃; pH=5.5;

DOI:10.1080/07328300500439413

upstream raw materials:

2-phenylethyl 2,3,4,2',3',4'-hexa-O-benzoyl-β-primeveroside

phenethyl 2,3,4,2',3',4'-O-hexaacetyl-β-D-xylopyranosyl-(1->6)-β-D-glucopyranoside

2-phenylethanol

phenethyl 2,3,4-tri-O-acetyl-β-D-glucopyranoside

Downstream raw materials:

primeverose

2-phenylethanol

1-O-β-D-xylopyranosyl-(1,6)-β-D-glucopyranoside