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1-O-trans-Cinnamoyl-beta-D-glucopyranose

Base Information
  • Chemical Name:1-O-trans-Cinnamoyl-beta-D-glucopyranose
  • CAS No.:40004-96-4
  • Molecular Formula:C15H18O7
  • Molecular Weight:310.304
  • Hs Code.:
  • ChEMBL ID:CHEMBL1215106
  • DSSTox Substance ID:DTXSID301286331
  • Metabolomics Workbench ID:50444
  • Nikkaji Number:J741.380G,J2.874.677F
  • Wikidata:Q27101829
1-O-trans-Cinnamoyl-beta-D-glucopyranose

Synonyms:1-O-trans-cinnamoyl-beta-D-glucopyranose

Suppliers and Price of 1-O-trans-Cinnamoyl-beta-D-glucopyranose
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
  • Packaging
  • price
Total 5 raw suppliers
Chemical Property of 1-O-trans-Cinnamoyl-beta-D-glucopyranose
Chemical Property:
  • XLogP3:0.1
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:5
  • Exact Mass:310.10525291
  • Heavy Atom Count:22
  • Complexity:391
Purity/Quality:

97.5% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O
  • Isomeric SMILES:C1=CC=C(C=C1)/C=C/C(=O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
Technology Process of 1-O-trans-Cinnamoyl-beta-D-glucopyranose

There total 5 articles about 1-O-trans-Cinnamoyl-beta-D-glucopyranose 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 pyridine; In water; at 35 ℃; for 5h;
DOI:10.1016/j.carres.2021.108332
Guidance literature:
With di-isopropyl azodicarboxylate; triphenylphosphine; In 1,4-dioxane; at 20 ℃; for 0.5h; stereoselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.0c01549
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