CAS 1013-88-3

Imina de benzofenona

Descripción:

Imina de benzofenona, con el número CAS 1013-88-3, es un compuesto orgánico caracterizado por su grupo funcional imina unido a una estructura de benzofenona. Típicamente aparece como una sustancia sólida o cristalina y es conocido por su papel en la síntesis orgánica y la fotociencia. El compuesto exhibe propiedades notables, como ser un posible absorbente de UV, lo que lo hace útil en diversas aplicaciones, incluyendo recubrimientos y plásticos. Imina de benzofenona puede participar en varias reacciones químicas, incluyendo adiciones nucleofílicas y cicloadiciones, debido a la naturaleza electrofílica del átomo de carbono en el grupo imina. También se reconoce por su capacidad para formar complejos estables con metales, lo que puede ser ventajoso en catálisis. Se deben tener en cuenta consideraciones de seguridad al manipular este compuesto, ya que puede representar riesgos para la salud al exponerse. En general, Imina de benzofenona es un compuesto versátil con implicaciones significativas tanto en entornos industriales como de investigación.

Fórmula: C₁₃H₁₁N

InChI: InChI=1S/C13H11N/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,14H

Clave InChI: InChIKey=SXZIXHOMFPUIRK-UHFFFAOYSA-N

SMILES: C(=N)(C1=CC=CC=C1)C2=CC=CC=C2

Sinónimos:

• 1,1-Diphenylmethanimine
• 1,1-Diphenylmethylenimine
• 90-97%
• Benzenemethanimine, α-phenyl-
• Benzenemethanimine,-phenyl-
• Benzhydrylideneamine
• Benzhydrylidenimine
• Benzophenone Imine
• Benzophenone Imine 97%
• Benzophenonimine
• Benzophone imine
• Diphenylketimine
• Diphenylmethanimine
• Iminodiphenylmethane
• Methylenimine, 1,1-diphenyl-

Benzophenone Imine

CAS: 1013-88-3

Fórmula: C₁₃H₁₁N

Pureza: >95.0%(GC)

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

Peso molecular: 181.24

Ref: 3B-B1912

Benzophenoneimine

CAS: 1013-88-3

Fórmula: C₁₃H₁₁N

Pureza: 98.0%

Forma y color: Liquid, Clear slightly dense colourless liquid

Peso molecular: 181.238

Ref: 10-F092251

Benzophenone imine, 95%, Stab.

CAS: 1013-88-3

Useful in the preparation of nitrile ylide dimers.Benzophenone imine as ammonia surrogate. As intermediate material for synthesis of organic chemicals. Catalytic enantioselective alkylation of the benzophenone imine of glycine t-butyl ester using phosphazene (Schwesinger) bases and chiral quaternar

Fórmula: C₁₃H₁₁N

Pureza: 95%

Forma y color: Clear colorless to yellow to yellow-brown, Liquid

Peso molecular: 181.24

Ref: 02-H30110

Benzenemethanimine, α-phenyl-

CAS: 1013-88-3

Fórmula: C₁₃H₁₁N

Pureza: 95%

Forma y color: Liquid

Peso molecular: 181.2331

Ref: IN-DA00046O

Diphenylmethanimine

CAS: 1013-88-3

Benzophenoneimine

Fórmula: C₁₃H₁₁N

Pureza: 97%

Peso molecular: 181.23

Ref: IN-DG115883

Benzophenone imine

CAS: 1013-88-3

Fórmula: C₁₃H₁₁N

Pureza: ≥ 95.0%

Forma y color: Colourless to yellow liquid

Peso molecular: 181.23

Ref: 7W-GT6995

Benzhydrylimine

CAS: 1013-88-3

Benzhydrylimine

Fórmula: C₁₃H₁₁N

Pureza: 95%

Forma y color: Liquid

Peso molecular: 181.23314

Ref: 54-OR42185

Benzophenone imine-Stabilized with 0.02% Hydroquinone

CAS: 1013-88-3

Benzophenone imine-Stabilized with 0.02% Hydroquinone (BPS-H) is an analytical reagent for the detection of halides in organic solutions. It reacts with the halide ion to form a benzophenone imine, which is stabilized by hydroquinone and can be detected by UV spectrophotometry at 330 nm. BPS-H can also be used for the synthesis of natural products containing nitrogen atoms and amines, such as ester hydrochloride. The mechanism of this reaction is based on hydrogen bonding between the protonated amine group and the carbonyl group in the benzophenone imine. The resulting product has a characteristic NMR spectrum that can be used to identify it as well as its purity. This compound also has chromatographic properties that make it suitable for use in thin layer chromatography (TLC).

Fórmula: C₁₃H₁₁N

Pureza: Min. 96.0 Area-%

Forma y color: Clear Liquid

Peso molecular: 181.23 g/mol

Ref: 3D-FB179202

Benzophenone imine

CAS: 1013-88-3

Benzophenone imine is a metabolite that is produced during the metabolism of benzophenones. It was first synthesized in 1887 by the reaction of copper chloride and benzene-1,2-diamine. The reaction solution was purified by fractional crystallization to give crystals of benzophenone imine hydrochloride (benzophenamine) as a white solid. The x-ray crystal structures were determined for two different forms, one with the 5-hydroxy group in the para position relative to the imine and one with it in the meta position. Benzophenone imine is an amide that has been shown to bind to 5-HT2 receptors, which are found primarily on neurons in the central nervous system. This binding leads to an increase in serotonin levels and an inhibition of glutamate release from nerve terminals. This inhibition can lead to infectious diseases such as herpes zoster.

Fórmula: C₁₃H₁₁N

Pureza: Min. 96.0 Area-%

Forma y color: Clear Liquid

Peso molecular: 181.23 g/mol

Ref: 3D-FB10487

Benzophenone Imine

Producto controlado

CAS: 1013-88-3

Fórmula: C₁₃H₁₁N

Forma y color: Neat

Peso molecular: 181.23

Ref: TR-B287290