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Benzenemethanimine, 3-methyl-α-phenyl-, also known as 3-methyl-α-phenylbenzenemethanimine or 3-methylbenzylideneamine, is an organic compound with the chemical formula C14H13N. It is a derivative of benzenemethanimine, featuring a methyl group attached to the 3-position of the phenyl ring. Benzenemethanimine, 3-methyl-a-phenyl- is characterized by its imine functional group, which consists of a carbon-nitrogen double bond, and is formed by the condensation of a primary amine with an aldehyde or ketone. Benzenemethanimine, 3-methyl-α-phenyl-, is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its reactivity and versatility in chemical transformations.

33497-37-9

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33497-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33497-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,9 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33497-37:
(7*3)+(6*3)+(5*4)+(4*9)+(3*7)+(2*3)+(1*7)=129
129 % 10 = 9
So 33497-37-9 is a valid CAS Registry Number.

33497-37-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-α-phenylbenzenemethanimine

1.2 Other means of identification

Product number -
Other names 3-methyl-benzophenone-imine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33497-37-9 SDS

33497-37-9Relevant academic research and scientific papers

Copper-catalyzed [2+3]-annulation of N-H imines with vinyl azides: Access to polyaryl 2: H -imidazoles

Zhu, Zhongzhi,Lin, Hanze,Liang, Baihui,Huang, Junjie,Liang, Wanyi,Chen, Lu,Huang, Yubing,Chen, Xiuwen,Li, Yibiao

supporting information, p. 5621 - 5624 (2020/06/19)

A practical method for the synthesis of 2H-imidazoles via a [2+3] annulation of N-H imines with vinyl azides using a copper catalyst is developed. In this conversion, environmentally friendly oxygen is used as the sole oxidant and N2 and H2O are the only by-products. The catalytic transformation, operating under mild conditions, is operationally simple and is considered as a readily available catalytic system having good substrate and functional compatibility with high atom-efficiency without the need for additional ligands or additives.

Hydrogen bond directed aerobic oxidation of amines via photoredox catalysis

Wang, Hongyu,Man, Yunquan,Wang, Kaiye,Wan, Xiuyan,Tong, Lili,Li, Na,Tang, Bo

supporting information, p. 10989 - 10992 (2018/10/08)

An application of H-bonding interactions for directing the α-C-H oxidation of amines to amides and amino-ketones catalyzed by an organic photocatalyst is reported. The high efficiency of this method is demonstrated by the aerobic oxidation of pyrrolidines, diarylamines and benzylamines bearing urea groups with high yields and a wide substrate scope.

Introducing Glycerol as a Sustainable Solvent to Organolithium Chemistry: Ultrafast Chemoselective Addition of Aryllithium Reagents to Nitriles under Air and at Ambient Temperature

Rodríguez-álvarez, María J.,García-álvarez, Joaquín,Uzelac, Marina,Fairley, Michael,O'Hara, Charles T.,Hevia, Eva

, p. 1720 - 1725 (2018/01/27)

Edging closer towards developing air and moisture compatible polar organometallic chemistry, the chemoselective and ultrafast addition of a range of aryllithium reagents to nitriles has been accomplished by using glycerol as a solvent, at ambient temperature in the presence of air, establishing a novel sustainable access to aromatic ketones. Addition reactions occur heterogeneously (“on glycerol conditions”), where the lack of solubility of the nitriles in glycerol and the ability of the latter to form strong intermolecular hydrogen bonds seem key to favouring nucleophilic addition over competitive hydrolysis. Remarkably, PhLi exhibits a greater resistance to hydrolysis working “on glycerol” conditions than “on water”. Introducing glycerol as a new solvent in organolithium chemistry unlocks a myriad of opportunities for developing more sustainable, air and moisture tolerant main-group-metal-mediated organic synthesis.

Synthesis of aryl ketones via decarboxylation of aromatic acids under solvothermal condition

Rai, K.M. Lokanatha,Babu, M. Suresh,Byrappa

experimental part, p. 1395 - 1396 (2012/08/27)

Aryl ketones were prepared by the condensation of aromatic carboxylic acids with alkyl/aryl nitrile via the decarboxylation of carboxylic acids under solvothermal condition. All the compounds were characterized by comparing with standard samples prepared by the known literature method.

On alkylideneamidosulfenyl chlorides and 1-thia-2-azoniaallene salts

Wirschun, Wolfgang G.,Hitzler, Martin G.,Jochims, Johannes C.,Groth, Ulrich

, p. 2627 - 2635 (2007/10/03)

X-Ray-diffraction analysis of 1Bu2C=N-SCl (4b) revealed an almost linear C=N=S unit with an S=N bond order of ca. 1.9 (Fig. 1), in agreement with the structure of a 1-thia-2-azoniaallene chloride. With SCl2 and SbCl5

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