10048-13-2
Product Name:
STERIGMATOCYSTIN
Formula:
C18H12O6
Synonyms:
3a,12c-Dihydro-8-hydroxy-6-methoxy-7H-furol[3′,2′:4,5]furo[2,3-c]xanthen-7-one;3a,12c-Dihydro-8-hydroxy-6-methoxy-7H-furol[3′,2′:4,5]furo[2,3-c]xanthen-7-one
Inquiry
CHEMICAL AND PHYSICAL PROPERTIES
Physical Description | Pale yellow solid; [HSDB] Yellow powder; [MSDSonline] |
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Color/Form | Pale-yellow crystals |
Melting Point | 246 °C with decomp |
Solubility | Insol in strong aq alkali; sparingly sol in most organic solvents; readily sol in dimethylsulfoxide, chloroform, pyridine |
Optical Rotation | SPECIFIC OPTICAL ROTATION: -398 DEG @ 20 °C/D (CHLOROFORM, 1%) |
Collision Cross Section | 163 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine] |
Other Experimental Properties | Forms deep-yellow color with aq sodium hydroxide and dark green-brown color with sulfuric acid; emits orange-red fluorescence in ultra-violet light |
Chemical Classes | Biological Agents -> Mycotoxins |
SAFETY INFORMATION
Signal word | Danger |
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Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 Health Hazard GHS08 |
GHS Hazard Statements |
H301:Acute toxicity,oral H351:Carcinogenicity |
Precautionary Statement Codes |
P201:Obtain special instructions before use. |
COMPUTED DESCRIPTORS
Molecular Weight | 324.3 g/mol |
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XLogP3 | 3.4 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 1 |
Exact Mass | 324.06338810 g/mol |
Monoisotopic Mass | 324.06338810 g/mol |
Topological Polar Surface Area | 74.2 Ų |
Heavy Atom Count | 24 |
Formal Charge | 0 |
Complexity | 562 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 2 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Sterigmatocystin is an organic heteropentacyclic compound whose skeleton comprises a xanthene ring system ortho-fused to a dihydrofuranofuran moiety. The parent of the class of sterigmatocystins. It has a role as a metabolite. It is functionally related to a dihydrodemethylsterigmatocystin.