CAS 1711-06-4
:m-Toluoyl chloride
Description:
m-Toluoyl chloride, also known as 3-toluoyl chloride, is an aromatic acyl chloride characterized by the presence of a toluene ring with a chlorine atom attached to the carbonyl group at the meta position. Its molecular formula is C8H7ClO, and it features a carbonyl (C=O) functional group, which contributes to its reactivity. This compound is typically a colorless to pale yellow liquid with a pungent odor, indicative of its reactivity and volatility. m-Toluoyl chloride is known for its role as an acylating agent in organic synthesis, particularly in the preparation of amides and esters. It is sensitive to moisture and can hydrolyze in the presence of water, forming m-toluic acid and hydrochloric acid. Due to its reactive nature, it should be handled with care, using appropriate safety measures to avoid skin and respiratory exposure. Its applications extend to the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, making it a valuable intermediate in chemical manufacturing.
Formula:C8H7ClO
InChI:InChI=1/C8H7ClO/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3
InChI key:InChIKey=YHOYYHYBFSYOSQ-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C1=CC(C)=CC=C1
Synonyms:- 3-Methylbenzoyl chloride
- 3-Toluoyl chloride
- Benzoyl chloride, 3-methyl-
- M-Methyl Benzoyl Chloride
- M-Toluyl Chloride
- Meta-Toluoyl Chloride
- NSC 97207
- Toluoyl chloride
- m-Methylbenzoyl chloride
- m-Toluenecarbonyl chloride
- m-Toluic acid chloride
- m-Toluoyl chloride
- toluoylchloride
- m-Toluoyl chloride(m-Toluicchloride)
- 3-Methylbenzenecarbonyl chloride
- 3-Methylbenzoic acid chloride
- m-Methylbenzoic acid chloride
- 3-toluoylchloride
- 3-ToluylChloride
- 3-METHYLBENZOYL CHLORIDE/M-TOLUOYL CHLORIDE
- meta Methyl benzoyl chloride
- Benzoyl chloride, 3-methyl-(9CI)
- See more synonyms
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Found 10 products.
m-Toluoyl chloride, 99%
CAS:<p>m-Toluoyl chloride has been used to derivatize the C1-C4 aliphatic amines for their determination in air by HPLC. It has been used in determination of atmospheric ammonia by denuder-sampling and HPLC-UV detection. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar p</p>Formula:C8H7ClOPurity:99%Color and Shape:Liquid, Clear colorless to pale yellowMolecular weight:154.59Benzoyl chloride, 3-methyl-
CAS:Formula:C8H7ClOPurity:97%Color and Shape:LiquidMolecular weight:154.5936m-Toluoyl Chloride
CAS:Formula:C8H7ClOPurity:>98.0%(GC)(T)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:154.59m-Toluoyl chloride
CAS:<p>m-Toluoyl chloride is a bioactive chemical.</p>Formula:C8H7ClOPurity:≥95%Color and Shape:Clear Colorless To Light Brown LiquidMolecular weight:154.59m-Toluoyl Chloride
CAS:Controlled Product<p>Applications m-Toluoyl Chloride is used as a reagent in the synthesis of glycine benzamides as oral GPR139 receptor agonists. m-Toluoyl Chloride is also used in the preparation of colchicine derivatives which have potent anticancer activity and reduced P-glycoprotein induction liability.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Dvorak, C.A., et al.: ACS Med. Chem. Lett., 6, 1015 (2015); Singh, B., et al.: Org. Biomol. Chem., 13, 5674 (2015)<br></p>Formula:C8H7ClOColor and Shape:NeatMolecular weight:154.59m-Toluoyl Chloride
CAS:<p>m-Toluoyl Chloride is an organic compound that is used as a reagent in the synthesis of a variety of chemical compounds. It is also used in clinical research to produce polyclonal antibodies. m-Toluoyl Chloride undergoes nucleophilic attack and forms amines, which are then acylated with chloroformates or carbonyl compounds to form molecules such as benzamides, pyridinium salts, and quaternary ammonium salts. The reaction mechanism for this process has been elucidated through molecular modeling and X-ray crystallography studies.</p>Formula:C8H7ClOPurity:Min. 95%Molecular weight:154.59 g/mol
