All About The 3-Methoxy 4-Methyl Methyl Benzoate

3-Methoxy 4-Methyl Methyl Benzoate is an oily acid that is biosynthesized by the Beilschmiedia tree. You can easily place your order online!

3-Methoxy commonly implies a chemical group or substituent where a methoxy (CH3O-) group is joined to a molecule at the third position of a carbon ring or chain. The number 3 implies the carbon atom where the methoxy group is joined.

A well-known compound, 3-Methoxy-4-Methyl Methyl Benzoate, is a special chemical compound with a particular chemical structure. Let’s discuss the point about the composition:

3-Methoxy

As the name implies, there is a methoxy (CH3O-) group joined to the benzene ring at the 3rd stand. Here, number 3 specifies the carbon atom on the benzene ring where the methoxy group is joined.

4-Methyl

The part of the name indicates that there is a methyl (CH3-) group joined to the benzene ring at the 4th stand. The number 4 implies the carbon atom on the benzene ring where the methyl group is joined.
Methyl Benzoate

The part of the name implies that the molecule rests on a benzoate group. The benzene ring itself is where the methoxy and methyl groups are joined.

3-Methoxy-4-methylbenzoic acid (3MMBA) is an oily acid that is biosynthesized by the Beilschmiedia tree. It has been exposed to antibacterial action against grammeme-positive and grammeme-negative microorganisms. 3MMBA also slows down the synthesis of bacterial fatty acids and inhibits the development of bacteria in vitro. The chromophore of 3MMBA is oxetane, which can be utilised as a sign for 3MMBA in chromatographic science.

Synthesis Pathway Design

The synthesis path for methyl 3-methoxy-4-methylbenzoate includes the reaction of 3-methoxy-4-methylbenzoic acid with methanol in the presence of a catalyst to outline the ester product.

Starting Stuff

3-methoxy-4-methylbenzoic acid, catalyst, and methanol
Reaction

• Step 1: Insert 3-methoxy-4-methylbenzoic acid and methanol into a response flask.
• Step 2: Add a channel, which includes hydrochloric acid or sulfuric acid, to the reaction flask.
• Step 3: Now, you can heat the reaction mixture under reflux conditions for numerous hours.
• Step 4: Let the mixture of the reactions cool, and then filter off any solid flaws.
• Step 5: Focus the filtrate under reduced pressure to find the crude product.
• Step 6: Cleanse the basic product by recrystallization or column chromatography to obtain pure methyl 3-methoxy-4-methylbenzoate.
Moreover, further research into the mixture of methyl 3-methoxy-4-methylbenzoate and its imitative could be performed. At last, further research could be performed into the usage of methyl 3-methoxy-4-methylbenzoate in the synthesis of different polymers and additional organic compounds.

General advice

Consult a medical doctor. Show the security of the data sheet to the doctor in attendance.

• If inhaled
If breathing in, move the individual into fresh air. If not breathing, present artificial respiration. Consult a medical doctor.
• Contact with the skin
Consult physicians and wash off with soap and lots of water.
• Contact with the eye contact
Rinse comprehensively with copious amounts of water for at least 15 minutes and seek advice from a physician.
• If swallowed
Never give something by mouth to an unaware person. Clean up the month with water. Consult a physician.
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