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293733

Sigma-Aldrich

Benzophenone imine

95%

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About This Item

Linear Formula:
(C6H5)2C=NH
CAS Number:
Molecular Weight:
181.23
Beilstein:
1100371
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

Quality Level

Assay

95%

form

liquid

refractive index

n20/D 1.618 (lit.)

bp

151-153 °C/10 mmHg (lit.)

density

1.08 g/mL at 25 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

N=C(c1ccccc1)c2ccccc2

InChI

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

InChI key

SXZIXHOMFPUIRK-UHFFFAOYSA-N

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General description

Benzophenone imine plays a vital role as an ammonia surrogate. It is primarily used as ammonia equivalents for the selective formation of protected primary amines. Benzophenone imine is useful as a synthetic intermediate, especially for the synthesis of glycine Schiff base.

Application

Benzophenone imine is useful for the preparation of nitrile yield dimers.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Suzanne Fergus et al.
The Journal of organic chemistry, 69(14), 4663-4669 (2004-07-03)
A series of novel hexaaryl diazatrienes 5 ("nitrile ylide dimers") were synthesized directly from the corresponding diaryl ketimines 12 and dichlorotoluenes 13 in a facile one-pot synthesis. The carbene character of the nitrile ylides was investigated by varying the substituents
Lukas Lohmeyer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(26), 5834-5845 (2020-02-06)
New redox-active 1,2,5,6-tetrakis(guanidino)-naphthalene compounds, isolable and storable in the neutral and deep-green dicationic redox states and oxidisable further in two one-electron steps to the tetracations, are reported. Protonation switches on blue fluorescence, with the fluorescence intensity (quantum yield) increasing with

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