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Viridin

Base Information Edit
  • Chemical Name:Viridin
  • CAS No.:3306-52-3
  • Deprecated CAS:1404-98-4
  • Molecular Formula:C20H16 O6
  • Molecular Weight:352.343
  • Hs Code.:
  • European Community (EC) Number:221-987-6
  • UNII:X5KJO207MO
  • DSSTox Substance ID:DTXSID00889372
  • Nikkaji Number:J7.714C
  • Wikipedia:Viridin
  • Wikidata:Q21099545
  • Metabolomics Workbench ID:103966
  • ChEMBL ID:CHEMBL2158159
  • Mol file:3306-52-3.mol
Viridin

Synonyms:viridin;viridin A;viridin B;viridin C

Suppliers and Price of Viridin
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • VIRIDIN 95.00%
  • 5MG
  • $ 498.25
  • American Custom Chemicals Corporation
  • VIRIDIN 95.00%
  • 1MG
  • $ 277.20
Total 4 raw suppliers
Chemical Property of Viridin Edit
Chemical Property:
  • Melting Point:245° (dec); mp 222-224° (dec); mp 200-205° (dec) 
  • Boiling Point:611.3±55.0 °C(Predicted) 
  • PKA:12.54±0.60(Predicted) 
  • Flash Point:323.5oC 
  • PSA:93.81000 
  • Density:1.51±0.1 g/cm3(Predicted) 
  • LogP:1.83110 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:1
  • Exact Mass:352.09468823
  • Heavy Atom Count:26
  • Complexity:688
Purity/Quality:

99% *data from raw suppliers

VIRIDIN 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12C(C(C(=O)C3=COC(=C31)C(=O)C4=C2C=CC5=C4CCC5=O)OC)O
  • Isomeric SMILES:C[C@]12[C@@H]([C@@H](C(=O)C3=COC(=C31)C(=O)C4=C2C=CC5=C4CCC5=O)OC)O
Technology Process of Viridin

There total 14 articles about Viridin 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: 48.0%

Guidance literature:
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; In dichloromethane; for 10h; Inert atmosphere; Sealed tube;
DOI:10.1021/jacs.7b02829

Reference yield: 46.0%

Guidance literature:
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; In dichloromethane; for 19h; Inert atmosphere; Sealed tube;
DOI:10.1021/jacs.7b02829
Guidance literature:
C19H14O6; With water; In dichloromethane; at 0 ℃; for 0.333333h; Inert atmosphere;
diazomethyl-trimethyl-silane; In dichloromethane; at 0 ℃;
DOI:10.1021/jacs.9b08577
upstream raw materials:

diazomethyl-trimethyl-silane

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