CAS 1013-88-3

Benzophenone imine

Description:

Benzophenone imine, with the CAS number 1013-88-3, is an organic compound characterized by its imine functional group attached to a benzophenone structure. It typically appears as a solid or crystalline substance and is known for its role in organic synthesis and photochemistry. The compound exhibits notable properties such as being a potential UV absorber, which makes it useful in various applications, including coatings and plastics. Benzophenone imine can participate in various chemical reactions, including nucleophilic additions and cycloadditions, due to the electrophilic nature of the carbon atom in the imine group. It is also recognized for its ability to form stable complexes with metals, which can be advantageous in catalysis. Safety considerations should be taken into account when handling this compound, as it may pose health risks upon exposure. Overall, benzophenone imine is a versatile compound with significant implications in both industrial and research settings.

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

Synonyms:

• 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

Purity: >95.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 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

Purity: 95%

Color and Shape: Clear colorless to yellow to yellow-brown, Liquid

Molecular weight: 181.24

Ref: 02-H30110

Benzophenoneimine

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Purity: 98.0%

Color and Shape: Liquid, Clear slightly dense colourless liquid

Molecular weight: 181.238

Ref: 10-F092251

Benzenemethanimine, α-phenyl-

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 181.2331

Ref: IN-DA00046O

Benzophenone imine

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Purity: ≥ 95.0%

Color and Shape: Colourless to yellow liquid

Molecular weight: 181.23

Ref: 7W-GT6995

Benzhydrylimine

CAS: 1013-88-3

Benzhydrylimine

Formula: C₁₃H₁₁N

Purity: 98%

Color and Shape: pale-yellow liquid

Molecular weight: 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

Purity: Min. 96.0 Area-%

Color and Shape: Clear Liquid

Molecular weight: 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

Purity: Min. 96.0 Area-%

Color and Shape: Clear Liquid

Molecular weight: 181.23 g/mol

Ref: 3D-FB10487

Benzophenone Imine

Controlled Product

CAS: 1013-88-3

Formula: C₁₃H₁₁N

Color and Shape: Neat

Molecular weight: 181.23

Ref: TR-B287290