CAS 1125-99-1

N-(ciclohex-1-en-1-il)pirrolidina

Descripción:

N-(ciclohex-1-en-1-il)pirrolidina, con el número CAS 1125-99-1, es un compuesto orgánico caracterizado por su estructura única que combina un anillo de pirrolidina con un sustituyente de ciclohexeno. Este compuesto presenta un heterociclo de cinco miembros que contiene nitrógeno (pirrolidina) y una parte de ciclohexeno, que introduce insaturación y contribuye a su reactividad. La presencia del doble enlace en el anillo de ciclohexeno puede dar lugar a diversas reacciones químicas, como adiciones electrofílicas o polimerización. N-(ciclohex-1-en-1-il)pirrolidina es típicamente un líquido incoloro a amarillo pálido a temperatura ambiente, exhibiendo solubilidad moderada en disolventes orgánicos. Su estructura molecular sugiere aplicaciones potenciales en síntesis orgánica, particularmente en el desarrollo de productos farmacéuticos o agroquímicos. Además, las propiedades del compuesto pueden verse influenciadas por factores como la hindrance estérica y los efectos electrónicos debido a las estructuras cíclicas, lo que lo convierte en un tema interesante para un estudio más profundo en química medicinal y ciencia de materiales.

Fórmula: C₁₀H₁₇N

InChI: InChI=1/C10H17N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h6H,1-5,7-9H2/p+1

Clave InChI: InChIKey=KTZNVZJECQAMBV-UHFFFAOYSA-N

SMILES: N1(CCCC1)C=2CCCCC2

Sinónimos:

• 1-(1-Cyclohexen-1-yl)pyrrolidine
• 1-(1-Cyclohexenyl)pyrrolidine
• 1-(1-Pyrrolidino)-1-cyclohexene
• 1-(1-Pyrrolidinyl)cyclohexene
• 1-(Cyclohex-1-en-1-yl)pyrrolidine
• 1-(Pyrrolidine-1-yl)-1-cyclohexene
• 1-Cyclohex-1-En-1-Ylpyrrolidinium
• 1-Pyrrolidino-1-cyclohexene
• 1-Pyrrolidinocyclohexene
• 1-Pyrrolidinyl-1-cyclohexene
• Cyclohexanone pyrrolidine enamine
• N-(1-Cyclohexen-1-yl)pyrrolidine
• N-(1-Cyclohexenyl)pyrrolidine
• NSC 29652
• Pyrrolidine, 1- (1-cyclohexen-1-yl)-
• 1-cyclohexenylpyrrolidine
• N-(cyclohex-1-en-1-yl)pyrrolidine
• N-Pyrrolidino-1-cyclohexene
• N-(1-CYCLOHEXEN-1-YL)-PYRROLIDIN
• 1-(1-PYRROLIDINO)CYCLOHEXENE 97%
• 1-Cyclohex-1-en-1-ylpyrrolidine
• 1-PYRROLIDINO-2-CYCLOHEXENE
• n-(cyclohexen-1-yl)pyrrolidine
• 1-(1-PYRROLIDINO)CYCLOHEXENE

1-Pyrrolidino-1-cyclohexene

CAS: 1125-99-1

Fórmula: C₁₀H₁₇N

Pureza: >97.0%(GC)(T)

Forma y color: White to Yellow to Green clear liquid

Peso molecular: 151.25

Ref: 3B-P1020

1-(1-Cyclohexen-1-yl)pyrrolidine, 97%

CAS: 1125-99-1

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Fórmula: C₁₀H₁₇N

Pureza: 97%

Forma y color: Clear, colorless to yellow, Liquid

Peso molecular: 151.25

Ref: 02-B25622

1-(Cyclohex-1-en-1-yl)pyrrolidine

CAS: 1125-99-1

Fórmula: C₁₀H₁₇N

Pureza: 97%

Forma y color: Liquid

Peso molecular: 151.2487

Ref: IN-DA003ENG

1-Cyclohex-1-en-1-ylpyrrolidine

CAS: 1125-99-1

1-Cyclohex-1-en-1-ylpyrrolidine

Pureza: ≥95%

Forma y color: Pale Yellow Liquid

Peso molecular: 151.25g/mol

Ref: 54-OR15935

1-Pyrrolidino-1-cyclohexene

CAS: 1125-99-1

Fórmula: C₁₀H₁₇N

Pureza: ≥97%

Forma y color: Liquid

Peso molecular: 151.253

Ref: 10-F099252

1-Pyrrolidino-1-cyclohexene

CAS: 1125-99-1

1-Pyrrolidino-1-cyclohexene (1PC) is a chemical compound that has been used clinically in the treatment of infections. The 1PC molecule is composed of a pyrrolidine ring and a cyclohexene ring, which are connected by an amide bond. The molecular geometry of 1PC can be regarded as a chair conformation with two hydrogen atoms occupying the two axial positions. It has been shown that 1PC inhibits the growth of bacteria by binding to chloride ions and catalyzing their conversion to reactive chloride species, which disrupts bacterial cells. The reaction mechanism for this process is similar to the Wolff-Kishner reduction, which involves dehydrating and deactivating the substrate. In addition, it was observed that 1PC inhibits bacterial growth by inhibiting protein synthesis through interaction energies with amino acids on ribosomes. This inhibition may be due to its ability to deprotect amino acids on ribosomes or

Fórmula: C₁₀H₁₇N

Pureza: Min. 96.5 Area-%

Forma y color: Clear Liquid

Peso molecular: 151.25 g/mol

Ref: 3D-FP165388