CAS 1711-06-4

Cloruro de m-toluílo

Descripción:

Cloruro de m-toluílo, también conocido como cloruro de 3-toluilo, es un cloruro acilo aromático caracterizado por la presencia de un anillo de tolueno con un átomo de cloro unido al grupo carbonilo en la posición meta. Su fórmula molecular es C8H7ClO, y presenta un grupo funcional carbonilo (C=O), que contribuye a su reactividad. Este compuesto es típicamente un líquido incoloro a amarillo pálido con un olor penetrante, indicativo de su reactividad y volatilidad. Cloruro de m-toluílo es conocido por su papel como agente acilante en la síntesis orgánica, particularmente en la preparación de amidas y ésteres. Es sensible a la humedad y puede hidrolizarse en presencia de agua, formando ácido m-toluico y ácido clorhídrico. Debido a su naturaleza reactiva, debe manejarse con cuidado, utilizando medidas de seguridad adecuadas para evitar la exposición cutánea y respiratoria. Sus aplicaciones se extienden a la síntesis de productos farmacéuticos, agroquímicos y otros compuestos orgánicos, lo que lo convierte en un intermediario valioso en la fabricación química.

Fórmula: C₈H₇ClO

InChI: InChI=1/C8H7ClO/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3

Clave InChI: InChIKey=YHOYYHYBFSYOSQ-UHFFFAOYSA-N

SMILES: C(Cl)(=O)C1=CC(C)=CC=C1

Sinónimos:

• 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)

m-Toluoyl chloride, 99%

CAS: 1711-06-4

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

Fórmula: C₈H₇ClO

Pureza: 99%

Forma y color: Liquid, Clear colorless to pale yellow

Peso molecular: 154.59

Ref: 02-B23914

Benzoyl chloride, 3-​methyl-

CAS: 1711-06-4

Fórmula: C₈H₇ClO

Pureza: 97%

Forma y color: Liquid

Peso molecular: 154.5936

Ref: IN-DA003S6G

m-Toluoyl chloride

CAS: 1711-06-4

m-Toluoyl chloride

Pureza: ≥95%

Peso molecular: 154.59g/mol

Ref: 54-BUP16970

m-Toluoyl Chloride

CAS: 1711-06-4

m-Toluoyl Chloride

Pureza: 98%

Peso molecular: 154.59g/mol

Ref: 54-OR1013920

m-Toluoyl Chloride

CAS: 1711-06-4

Fórmula: C₈H₇ClO

Pureza: >98.0%(GC)(T)

Forma y color: Colorless to Light yellow to Light orange clear liquid

Peso molecular: 154.59

Ref: 3B-T0309

m-Toluoyl chloride

CAS: 1711-06-4

m-Toluoyl chloride is a bioactive chemical.

Fórmula: C₈H₇ClO

Pureza: ≥95%

Forma y color: Clear Colorless To Light Brown Liquid

Peso molecular: 154.59

Ref: TM-T7850

m-Toluoyl Chloride

CAS: 1711-06-4

Fórmula: C₈H₇ClO

Peso molecular: 154.59

Ref: 4Z-T-6976

m-Toluoyl Chloride

Producto controlado

CAS: 1711-06-4

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.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Dvorak, C.A., et al.: ACS Med. Chem. Lett., 6, 1015 (2015); Singh, B., et al.: Org. Biomol. Chem., 13, 5674 (2015)

Fórmula: C₈H₇ClO

Forma y color: Neat

Peso molecular: 154.59

Ref: TR-T536255

m-Toluoyl chloride

CAS: 1711-06-4

Fórmula: C₈H₇ClO

Pureza: 97%

Forma y color: Liquid

Peso molecular: 154.59

Ref: 10-F095026

m-Toluoyl Chloride

CAS: 1711-06-4

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.

Fórmula: C₈H₇ClO

Pureza: Min. 95%

Peso molecular: 154.59 g/mol

Ref: 3D-BAA71106