Newblue CHEM-USNIC ...

Newblue CHEM-USNIC ACID

Newblue CHEM-USNIC ACID

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1 Kilogram

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  • Min.Order :1 Kilogram
  • Purity: 98%
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Keywords

125-46-2 USNIC ACID USNIC ACID

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  • ProductionCapacity:10|Kilogram|Month
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Details:

 
Product Name: USNIC ACID
Synonyms: (+-)-uanicacid;2,6-diacetyl-1,;2,6-diacetyl-1,2,3,9b-tetrahydro-7,9-dihydroxy-8,9b-dimethyldibenzofuran-1,3-dione;2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyl-1,3(2h,9bh)-dibenzofurandione;3(2H,9bH)-Dibenzofurandione,2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyl-1;9bh)-dibenzofurandione,2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyl-3(2h;usninsaeure;usno
CAS: 125-46-2
MF: C18H16O7
MW: 344.32
EINECS: 231-456-0
Product Categories: Miscellaneous Natural Products;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Inhibitors
Mol File: 125-46-2.mol
USNIC ACID Structure
USNIC ACID Chemical Properties
Melting point 200°C
alpha D16 +509.4° (c = 0.697 in chloroform)
refractive index 495 ° (C=0.7, CHCl3)
Merck 9893
CAS DataBase Reference 125-46-2(CAS DataBase Reference)
EPA Substance Registry System 1,3(2H,9bH)-Dibenzofurandione, 2,6-diacetyl-7,9-dihydroxy- 8,9b-dimethyl-(125-46-2)
Safety Information
Hazard Codes T,N
Risk Statements 25-50/53
Safety Statements 22-24/25-61-60-45
RTECS HP5270000
Hazardous Substances Data 125-46-2(Hazardous Substances Data)
MSDS Information
USNIC ACID Usage And Synthesis
Uses antibacterial
Uses Usnic acid is a major metabolite from a number of lichen and fungal species and is perhaps one of the longest known microbial metabolites, first isolated in 1844. Usnic acid exhibits a broad range of biological activity, indeed it is easier to list the bioassays in which it does not exhibit activity. More often than not, potency is low and of limited value. Usnic acid is an important metabolite for dereplication in discovery research programs.
Definition ChEBI: A member of the class of dibenzofurans that is dibenzo[b,d]furan-1(9bH)-one substituted by acetyl groups at positions 2 and 6, hydroxy groups at positions 3 and 7 and methyl groups at positions 8 and 9b.

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