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Vimalin

Base Information
  • Chemical Name:Vimalin
  • CAS No.:143729-77-5
  • Molecular Formula:C16H22O7
  • Molecular Weight:326.346
  • Hs Code.:
  • UNII:N08S5L5SV5
  • Nikkaji Number:J15.849F,J440.225A
  • Wikidata:Q27284335
Vimalin

Synonyms:Vimalin;Vimalin, (-)-;Glucopyranoside, p-methoxycinnamyl;UNII-N08S5L5SV5;N08S5L5SV5;143729-77-5;19764-36-4;beta-D-Glucopyranoside, 3-(4-methoxyphenyl)-2-propenyl;beta-D-Glucopyranoside, 3-(4-methoxyphenyl)-2-propen-1-yl;beta-D-Glucopyranoside, (2E)-3-(4-methoxyphenyl)-2-propen-1-yl;3-(4-Methoxyphenyl)-2-propenyl beta-D-glucopyranoside;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]oxane-3,4,5-triol;.beta.-D-Glucopyranoside, 3-(4-methoxyphenyl)-2-propenyl;Q27284335;.BETA.-D-GLUCOPYRANOSIDE, (2E)-3-(4-METHOXYPHENYL)-2-PROPEN-1-YL;.BETA.-D-GLUCOPYRANOSIDE, 3-(4-METHOXYPHENYL)-2-PROPEN-1-YL

Suppliers and Price of Vimalin
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of Vimalin
Chemical Property:
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:6
  • Exact Mass:326.13655304
  • Heavy Atom Count:23
  • Complexity:367
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O
  • Isomeric SMILES:COC1=CC=C(C=C1)/C=C/CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
Technology Process of Vimalin

There total 8 articles about Vimalin 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:
Guidance literature:
With α-L-rhamnosyl-β-D-glucosidase from Aspergillus niger; In aq. phosphate buffer; dimethyl sulfoxide; at 35 ℃; for 8h; pH=5; Enzymatic reaction;
DOI:10.1002/cssc.201700136
Guidance literature:
With phosphate buffer; β-glucosidase; at 30 ℃; for 24h; pH=5;
DOI:10.1248/cpb.52.270
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