4-Methylanisole

4-Methylanisole Structure
4-Methylanisole structure
Common Name 4-Methylanisole
CAS Number 104-93-8 Molecular Weight 122.164
Density 0.96 Boiling Point 174 ºC
Molecular Formula C8H10O Melting Point -32°C
MSDS Chinese USA Flash Point 53 ºC
Symbol GHS02 GHS07 GHS08
GHS02, GHS07, GHS08
Signal Word Warning

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. Surprisingly, the odoriferous principle(s) underlying its uniqu...

Developmental immunotoxicity testing of 4-methyl anisole.

Regul Toxicol Pharmacol 72 , 379-85, (2015)

The developmental immunotoxicity of 4-methyl anisole (4MA) was investigated in the rat. Four study designs were used, with either premating or post-weaning onset of exposure, continued to postnatal day 50, and with or without additional oral gavage of pups fr...

Individual solvent/solute interactions through social isomerism.

J. Am. Chem. Soc. 125(46) , 13981-3, (2003)

Reversible coencapsulation of a solute molecule and a single solvent molecule takes place in solution at ambient temperature. Two isomeric complexes are formed (social isomers), and their relative energies are assessed by NMR methods. Intermolecular interacti...

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 1.0 kcal/mol lower barrier than abstraction from a simple ben...

Occurrence of aromatic methyl migration (NIH-shift) during oxidation of p-methylanisole by hemin-thiolester complex as a cytochrome P-450 model.

Biochem. Biophys. Res. Commun. 108(4) , 1649-54, (1982)

Four-week toxicity study of 4-methoxytoluene in rats.

Toxicol. Lett. 73(3) , 209-12, (1994)

4-Methoxytoluene was given by gavage to 4 groups of 20 rats at dosage levels of 0, 40, 120 or 240 mg kg-1 body weight/day for 4 weeks. There was a statistically significant decrease in serum creatinine and urea in the intermediate and high dose group for both...

Vibrations and theoretical calculations of p-methylanisole in the first electronically excited S1 and ionic ground D0 states.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 67(3-4) , 824-9, (2007)

One-color (1C), two-color (2C) resonant two-photon ionization (R2PI), and mass analyzed threshold ionization (MATI) methods have been applied to study the S(1)<--S(0) transition and threshold ionization of p-methylanisole. The excitation energy of the S(1)<--...

Solubilization Site of Organic Perfume Molecules in Sodium Dodecyl Sulfate Micelles: New Insights from Proton NMR Studies.

J. Colloid. Interface Sci. 225(1) , 32-38, (2000)

The site of incorporation of solubilizates in sodium dodecyl sulfate (SDS) micellar systems has been investigated by proton NMR spectroscopy. The solubilizate molecules chosen for the present study are phenol, 4-methylphenol, 4-allyl-2-methoxyphenol, anisole,...

A concise synthesis of (+/-)-cacalol.

J. Org. Chem. 73(13) , 5177-9, (2008)

A simple synthesis of the natural product cacalol has been developed that proceeds in seven steps and 21-25% overall yield. Ortho-lithiation of 4-methylanisole and alkylation with 5-iodo-1-pentene, followed by intramolecular Friedel-Crafts alkylation, gave 5-...