2-Methylanisole structure
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Common Name | 2-Methylanisole | ||
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CAS Number | 578-58-5 | Molecular Weight | 122.164 | |
Density | 0.9±0.1 g/cm3 | Boiling Point | 171.0±0.0 °C at 760 mmHg | |
Molecular Formula | C8H10O | Melting Point | 170-172 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 51.7±0.0 °C | |
Symbol |
GHS02 |
Signal Word | Warning |
Use of 2-Methylanisole2-Methylanisole is a monomethoxybenzene and acts as an intermediate for the preparation of compounds with methylhydroquinone core [1]. |
Name | 2-Methylanisole |
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Synonym | More Synonyms |
Description | 2-Methylanisole is a monomethoxybenzene and acts as an intermediate for the preparation of compounds with methylhydroquinone core [1]. |
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Related Catalog | |
References |
Density | 0.9±0.1 g/cm3 |
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Boiling Point | 171.0±0.0 °C at 760 mmHg |
Melting Point | 170-172 °C(lit.) |
Molecular Formula | C8H10O |
Molecular Weight | 122.164 |
Flash Point | 51.7±0.0 °C |
Exact Mass | 122.073166 |
PSA | 9.23000 |
LogP | 2.59 |
Vapour Pressure | 1.9±0.3 mmHg at 25°C |
Index of Refraction | 1.494 |
Storage condition | Flammables area |
Water Solubility | immiscible |
Symbol |
GHS02 |
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Signal Word | Warning |
Hazard Statements | H226 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | F |
Risk Phrases | R10 |
Safety Phrases | S16 |
RIDADR | UN 1993 3/PG 3 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 3 |
HS Code | 29093090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2909309090 |
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Summary | 2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Identification of odorants in frankincense (Boswellia sacra Flueck.) by aroma extract dilution analysis and two-dimensional gas chromatography-mass spectrometry/olfactometry.
Phytochemistry 109 , 66-75, (2014) Frankincense has been known, traded and used throughout the ages for its exceptional aroma properties, and is still commonly used in both secular and religious settings to convey a pleasant odor. Surp... |
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An assessment of the reaction energetics for cytochrome P450-mediated reactions.
Arch. Biochem. Biophys. 385(1) , 220-30, (2001) Regioselectivity is used to determine the absolute energetic differences for four different reactions catalyzed by P450. Abstraction of a hydrogen from a benzylic carbon containing a chlorine has a 1.... |
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(+)- and (-)-mutisianthol: first total synthesis, absolute configuration, and antitumor activity.
J. Org. Chem. 74(6) , 2561-6, (2009) The first synthesis of the natural product (+)-mutisianthol was accomplished in 11 steps and in 21% overall yield from 2-methylanisole. The synthesis of its enantiomer was also performed in a similar ... |
1-Methoxy-2-methylbenzene |
2-Methylanisole |
EINECS 209-426-3 |
MFCD00008373 |
Methyl 2-methylphenyl ether |
Benzene, 1-methoxy-2-methyl- |