| Weight | 126.111 g/mol |
|---|---|
| Formula | C6H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
phloroglucinol (626-71-1, 108-73-6)
Spasfon-Lyoc · Benzene-1,3,5-triol · 1,3,5-Benzenetriol
Score:
#3450 in Biology
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#4308 in Chemistry
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- Analysis of Proanthocyanidin Cleavage Products Following Acid-Catalysis in the Presence of Excess Phloroglucinol (Journal of Agricultural and Food Chemistry, 2001)
- Phloroglucinol compounds of natural origin (Natural Product Reports, 2006)
- Randomized trial of the efficacy of tamsulosin, nifedipine and phloroglucinol in medical expulsive therapy for distal ureteral calculi. (The Journal of Urology, 2005)
- Phloroglucinol Based Microporous Polymeric Organic Frameworks with OH Functional Groups and High CO2 Capture Capacity (Chemistry of Materials, 2011)
- A simplified, colorimetric micromethod for xylose in serum or urine, with phloroglucinol. (Clinical Chemistry, 1979)
- Studies in relation to Biosynthesis. I. Some possible routes to derivatives of Orcinol and Phloroglucinol (Australian Journal of Chemistry, 1953)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Spasfon-Lyoc
- Benzene-1,3,5-triol
- 1,3,5-Benzenetriol
- Spassirex
-
SMILESC1=C(C=C(C=C1O)O)O
-
InChIKeyQCDYQQDYXPDABM-UHFFFAOYSA-N
- Pubchem - phloroglucinol
- Wikipedia - phloroglucinol
Phloroglucinol is an organic compound that is used in the synthesis of pharmaceuticals and explosives. It is a phenol derivative with antispasmodic properties that is used primarily as a laboratory reagent. In 1855, phloroglucinol was first prepared from phloretin by the Austrian chemist Heinrich Hlasiwetz (18251875), who is remembered for his chemical analysis of phloroglucinol.
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phloroglucinol
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