CAS 1013-88-3

Immina di benzofenone

Descrizione:

Immina di benzofenone, con il numero CAS 1013-88-3, è un composto organico caratterizzato dal suo gruppo funzionale immina legato a una struttura di benzofenone. Appare tipicamente come una sostanza solida o cristallina ed è noto per il suo ruolo nella sintesi organica e nella fotochimica. Il composto presenta proprietà notevoli, come quella di essere un potenziale assorbitore di UV, il che lo rende utile in varie applicazioni, tra cui rivestimenti e plastiche. Immina di benzofenone può partecipare a varie reazioni chimiche, comprese le aggiunte nucleofile e le cicloadizioni, a causa della natura elettrofila dell'atomo di carbonio nel gruppo immina. È anche riconosciuto per la sua capacità di formare complessi stabili con i metalli, il che può essere vantaggioso nella catalisi. Devono essere prese in considerazione le questioni di sicurezza quando si maneggia questo composto, poiché può comportare rischi per la salute in caso di esposizione. In generale, Immina di benzofenone è un composto versatile con implicazioni significative sia in contesti industriali che di ricerca.

Formula: C₁₃H₁₁N

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

InChI key: InChIKey=SXZIXHOMFPUIRK-UHFFFAOYSA-N

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

Sinonimi:

• 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

Formula: C₁₃H₁₁N

Purezza: >95.0%(GC)

Colore e forma: Colorless to Light orange to Yellow clear liquid

Peso molecolare: 181.24

Ref: 3B-B1912

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

Formula: C₁₃H₁₁N

Purezza: 95%

Colore e forma: Clear colorless to yellow to yellow-brown, Liquid

Peso molecolare: 181.24

Ref: 02-H30110

Benzenemethanimine, α-phenyl-

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Purezza: 95%

Colore e forma: Liquid

Peso molecolare: 181.2331

Ref: IN-DA00046O

Benzophenone imine

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Purezza: ≥ 95.0%

Colore e forma: Colourless to yellow liquid

Peso molecolare: 181.23

Ref: 7W-GT6995

Benzophenoneimine

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Purezza: 98.0%

Colore e forma: Liquid, Clear slightly dense colourless liquid

Peso molecolare: 181.238

Ref: 10-F092251

Benzhydrylimine

CAS: 1013-88-3

Benzhydrylimine

Formula: C₁₃H₁₁N

Purezza: 98%

Colore e forma: pale-yellow liquid

Peso molecolare: 181.23g/mol

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).

Formula: C₁₃H₁₁N

Purezza: Min. 96.0 Area-%

Colore e forma: Clear Liquid

Peso molecolare: 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.

Formula: C₁₃H₁₁N

Purezza: Min. 96.0 Area-%

Colore e forma: Clear Liquid

Peso molecolare: 181.23 g/mol

Ref: 3D-FB10487

Benzophenone Imine

Prodotto controllato

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Colore e forma: Neat

Peso molecolare: 181.23

Ref: TR-B287290