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Brazilin

Base Information Edit
  • Chemical Name:Brazilin
  • CAS No.:474-07-7
  • Deprecated CAS:22562-62-5
  • Molecular Formula:C16H14O5
  • Molecular Weight:286.284
  • Hs Code.:29329990
  • European Community (EC) Number:207-477-6
  • UNII:FZ39SW1K10
  • DSSTox Substance ID:DTXSID80883393
  • Nikkaji Number:J631.276D
  • Wikipedia:Brazilin
  • Wikidata:Q3643873
  • Metabolomics Workbench ID:53020
  • ChEMBL ID:CHEMBL598951
  • Mol file:474-07-7.mol
Brazilin

Synonyms:brasilin;brazilin

Suppliers and Price of Brazilin
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
  • Usbiological
  • Brazilin
  • 10mg
  • $ 490.00
  • DC Chemicals
  • Brazilin >98%,StandardReferencesGrade
  • 20 mg
  • $ 280.00
  • Crysdot
  • Brazilin 97%
  • 10mg
  • $ 250.00
  • Crysdot
  • Brazilin 97%
  • 25mg
  • $ 480.00
  • Cayman Chemical
  • Brazilin ≥98%
  • 1mg
  • $ 28.00
  • Cayman Chemical
  • Brazilin ≥98%
  • 5mg
  • $ 123.00
  • Cayman Chemical
  • Brazilin ≥98%
  • 10mg
  • $ 204.00
  • Cayman Chemical
  • Brazilin ≥98%
  • 50mg
  • $ 879.00
  • Biosynth Carbosynth
  • Brazilin
  • 250 mg
  • $ 925.00
  • Biosynth Carbosynth
  • Brazilin
  • 25 mg
  • $ 160.00
Total 65 raw suppliers
Chemical Property of Brazilin Edit
Chemical Property:
  • Vapor Pressure:3.44E-13mmHg at 25°C 
  • Melting Point:156-157oC 
  • Refractive Index:1.774 
  • Boiling Point:555.8 °C at 760 mmHg 
  • Flash Point:289.9 °C 
  • PSA:90.15000 
  • Density:1.604 g/cm3 
  • LogP:1.61490 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:0
  • Exact Mass:286.08412354
  • Heavy Atom Count:21
  • Complexity:416
Purity/Quality:

98%,99%, *data from raw suppliers

Brazilin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C2=CC(=C(C=C2C3C1(COC4=C3C=CC(=C4)O)O)O)O
  • Isomeric SMILES:C1C2=CC(=C(C=C2[C@H]3[C@@]1(COC4=C3C=CC(=C4)O)O)O)O
  • Description Brazilin is an isoflavonoid originally isolated from C. sappan that has diverse biological activities, including neuroprotective, anti-inflammatory, antibacterial, and antioxidant properties. Brazilin inhibits Aβ (1-42) fibrillogenesis (IC50 = 1.5 μM) more potently than (-)-epigallocatechin gallate , cucurmin , and resveratrol (Item Nos. 10004235 | 70675). It also prevents remodeling of mature Aβ (1-42) fibrils. Brazilin inhibits the production of cytokines, including PGE2 and TNF-α (IC50s = 12.6 and 87.2 μM). It is effective against Gram-positive and Gram-negative bacteria with MICs ranging from 31.3 to 250 μg/ml. In addition, brazilin inhibits osteoclast differentiation mediated by RANKL and is protective against LPS-induced osteoporosis in mice at a dose of 100 mg/kg.
  • Uses Brazilin is a hair dyeing composition that comprises a natural dye and fatty amine. inhibits platelet aggregation, PLA2, PKC, protein phosphatase, insulin receptor kinase, nitric oxide synthase, antineoplastic Chiefly as a dye. Has also been recommended as indicator in acid-base titrations; acids = yellow, alkalies = carmine-red.
Technology Process of Brazilin

There total 104 articles about Brazilin 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 hydrogenchloride; water; In acetonitrile; at 80 ℃;
DOI:10.1016/j.bmcl.2011.06.066
Guidance literature:
With boron tribromide; In dichloromethane; at -78 - 20 ℃; for 18h; Inert atmosphere;
Guidance literature:
With boron tribromide; In dichloromethane; at -78 - 20 ℃; for 18h;
DOI:10.1016/j.tetlet.2020.152052
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