7786-61-0
Product Name:
4-Hydroxy-3-methoxystyrene
Formula:
C9H10O2
Synonyms:
2-Methoxy-4-vinylphenol;4-Vinyl guaiacol
Inquiry
CHEMICAL AND PHYSICAL PROPERTIES
Physical Description | Colourless or pale straw oily liquid, powerful, spicy, clove-like roasted peanut odour |
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Solubility | insoluble in water; soluble in oils |
Density | 1.090-1.096 |
Refractive Index | 1.534-1.538 |
Kovats Retention Index | 1272 1282 1280 1295 1294 1286 1282 1286 1291 1282 1284 1287 1284 1274 1277 1284 1311 1289 1278 1300 1286 1289 1289 1299 1280 1313.1 1277 1311 1311 1289 1285 1279 1297 1277 1280 1280 1280 1286 1289 1293.1 1280 1280 1280 1280 |
SAFETY INFORMATION
Signal word | Danger |
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Pictogram(s) |
Corrosion Corrosives GHS05 |
GHS Hazard Statements |
H314:Skin corrosion/irritation |
Precautionary Statement Codes |
P260:Do not breathe dust/fume/gas/mist/vapours/spray. P280:Wear protective gloves/protective clothing/eye protection/face protection. P363:Wash contaminated clothing before reuse. P303+P361+P353:IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
COMPUTED DESCRIPTORS
Molecular Weight | 150.17 g/mol |
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XLogP3 | 2.4 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 2 |
Exact Mass | 150.068079557 g/mol |
Monoisotopic Mass | 150.068079557 g/mol |
Topological Polar Surface Area | 29.5 Ų |
Heavy Atom Count | 11 |
Formal Charge | 0 |
Complexity | 134 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
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
2-methoxy-4-vinylphenol is a member of the class of phenols that is guaiacol in which the hydrogen para- to the hydroxy group is replaced by a vinyl group. It has a role as a pheromone, a flavouring agent and a plant metabolite.