CAS 18997-19-8

Pivalato de clorometilo

Descripción:

Pivalato de clorometilo, con el número CAS 18997-19-8, es un compuesto orgánico caracterizado por su grupo funcional éster y la presencia de un grupo clorometilo. Se deriva del ácido pivalico, que es un ácido carboxílico de cadena ramificada, y presenta un sustituyente clorometilo que mejora su reactividad. Este compuesto es típicamente un líquido incoloro a amarillo pálido con un olor distintivo. Es soluble en disolventes orgánicos pero tiene una solubilidad limitada en agua debido a su naturaleza hidrofóbica. Pivalato de clorometilo se utiliza principalmente como un intermedio en la síntesis orgánica, particularmente en la producción de productos farmacéuticos y agroquímicos. Su reactividad se atribuye a la presencia del grupo clorometilo, que puede participar en reacciones de sustitución nucleofílica. Se requieren precauciones de seguridad al manipular este compuesto, ya que puede representar riesgos para la salud, incluyendo irritación de la piel y del sistema respiratorio. Se deben seguir protocolos adecuados de almacenamiento y manipulación para mitigar cualquier peligro potencial asociado con su uso.

Fórmula: C₆H₁₁ClO₂

InChI: InChI=1S/C6H11ClO2/c1-6(2,3)5(8)9-4-7/h4H2,1-3H3

Clave InChI: InChIKey=GGRHYQCXXYLUTL-UHFFFAOYSA-N

SMILES: C(C(C)(C)C)(OCCl)=O

Sinónimos:

• (2,2-Dimethyl-1-oxopropoxy)methyl chloride
• 2,2-Dimethylpropionic acid chloromethyl ester
• Chloromethyl 2,2-dimethylpropanoate
• Chloromethyl 2,2-dimethylpropionate
• Chloromethyl Pivalate [Amino-Protecting Agent]
• Chloromethyl trimethylacetate
• Methanol, chloro-, pivalate
• POM-Cl
• Pivalic acid, chloromethyl ester
• Pivaloyloxymethyl chloride
• Propanoic acid, 2,2-dimethyl-, chloromethyl ester
• [(tert-Butylcarbonyl)oxy]methyl chloride

Chloromethyl Pivalate [Amino-Protecting Agent]

CAS: 18997-19-8

Fórmula: C₆H₁₁ClO₂

Pureza: >99.0%(GC)

Forma y color: Colorless to Almost colorless clear liquid

Peso molecular: 150.60

Ref: 3B-P1012

Chloromethyl pivalate, 97%

CAS: 18997-19-8

Chloromethyl pivalate acts as an intermediate in the synthesis of active pharmaceutical ingredients. It is also involved in the acylation reaction with 9-(2-phosphonylmethoxyethyl)adenine. It serves as a protecting reagent used for the N-protection of amines. It is also employed in the preparation

Fórmula: C₆H₁₁ClO₂

Pureza: 97%

Forma y color: Clear colorless to pale yellow, Liquid

Peso molecular: 150.60

Ref: 02-A11967

Propanoic acid, 2,2-dimethyl-, chloromethyl ester

CAS: 18997-19-8

Fórmula: C₆H₁₁ClO₂

Pureza: 98%

Forma y color: Liquid

Peso molecular: 150.6033

Ref: IN-DA002E7E

Chloromethyl pivalate

CAS: 18997-19-8

Chloromethyl pivalate

Pureza: 99%

Forma y color: Liquid

Peso molecular: 150.60g/mol

Ref: 54-OR924060

Chloromethyl pivalate

CAS: 18997-19-8

Fórmula: C₆H₁₁ClO₂

Pureza: 99.0%

Forma y color: Liquid

Peso molecular: 150.6

Ref: 10-F035584

Chloromethyl Pivalate

Producto controlado

CAS: 18997-19-8

Applications Chloromethyl Pivalate is used in the synthesis of oxazolines used in the preparation of imidazolium triflates. Also used in the synthesis of Src Kinase inhibitors used as anti-tumor agents.
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 Glorius, F. et al.: Chem. Comm., 22, 2704 (2002); Hennequin, L. et al.: J. Med. Chem., 49, 6465 (2006);

Fórmula: C₆H₁₁ClO₂

Forma y color: Neat

Peso molecular: 150.6

Ref: TR-C369675

Chloromethyl Pivalate

CAS: 18997-19-8

Fórmula: C₆H₁₁ClO₂

Peso molecular: 150.6

Ref: ST-EA-CP-P290001

Chloromethyl pivalate

CAS: 18997-19-8

Chloromethyl pivalate is an antimicrobial agent that belongs to the group of acyclic nucleoside phosphonates. It has been shown to inhibit the enzyme pyrazinoic acid synthase, which is involved in the biosynthesis of the pyrazinoic acid. Chloromethyl pivalate has significant cytotoxicity against cancer cells and can be used for the treatment of infectious diseases such as tuberculosis and leishmaniasis. Chloromethyl pivalate inhibits cell growth by binding to DNA and inhibiting protein synthesis. This drug also inhibits intermolecular hydrogen bonding, which may lead to its inhibition of bacterial growth.

Fórmula: C₆H₁₁ClO₂

Pureza: Min. 95%

Forma y color: Colorless Slightly Yellow Clear Liquid

Peso molecular: 150.6 g/mol

Ref: 3D-FC07730