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Benzoic acid, 4-[(diphenylmethylene)amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102222-52-6

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102222-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102222-52-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,2 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102222-52:
(8*1)+(7*0)+(6*2)+(5*2)+(4*2)+(3*2)+(2*5)+(1*2)=56
56 % 10 = 6
So 102222-52-6 is a valid CAS Registry Number.

102222-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(benzhydrylideneamino)benzoate

1.2 Other means of identification

Product number -
Other names 4-benzhydrylidenamino-benzoic acid ethyl ester

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:102222-52-6 SDS

102222-52-6Downstream Products

102222-52-6Relevant academic research and scientific papers

Copper-Catalysed Electrophilic Amination of Aryl(alkenyl) Boronic Acids with Nitrogen-Containing Hypervalent Iodine (III) Reagent

Hu, Yuanyuan,Zheng, Songlin,Fan, Wu,Yuan, Weiming

supporting information, p. 4701 - 4707 (2021/08/23)

A copper-catalysed electrophilic N-imination of aryl(alkenyl) boronic acids with a stable hypervalent iodine(III) reagent containing a transferable (diarylmethylene)amino group is developed. The electrophilic C?N cross-coupling reaction proceeds smoothly at room temperature under oxidant-free and base-free conditions, which is further characterized by the broad functional group compatibility, thereof, extending the N-electrophile scope of electrophilic C?N cross-coupling outside the limitation of N?O and N?Cl reagents. (Figure presented.).

Photocatalytic and Chemoselective Transfer Hydrogenation of Diarylimines in Batch and Continuous Flow

Van As, Dean J.,Connell, Timothy U.,Brzozowski, Martin,Scully, Andrew D.,Polyzos, Anastasios

supporting information, p. 905 - 908 (2018/02/22)

A visible-light photocalytic method for the chemoselective transfer hydrogenation of imines in batch and continuous flow is described. The reaction utilizes Et3N as both hydrogen source and single-electron donor, enabling the selective reduction of imines derived from diarylketimines containing other reducible functional groups including nitriles, halides, esters, and ketones. The dual role of Et3N was confirmed by fluorescence quenching measurements, transient absorption spectroscopy, and deuterium-labeling studies. Continuous-flow processing facilitates straightforward scale-up of the reaction.

A facile access for the C-N bond formation by transition metal-free oxidative coupling of benzylic C-H bonds and amides

Liu, Jie,Zhang, Heng,Yi, Hong,Liu, Chao,Lei, Aiwen

, p. 1323 - 1328 (2015/08/11)

Using 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) as the oxidant, we communicate an efficient oxidative C-N coupling of benzylic C-H bonds with amides to afford a series of amination products in good yields. A wide range of functional groups as well as various sulfonamides and carboxamides are well tolerated. Moreover, this reaction involves both the challenging C-H functionalization and C-N bond formation.

SYNTHESIS OF KETIMINES VIA PALLADIUM COMPLEX-CATALYZED CROSS-COUPLING OF IMIDOYL CHLORIDES WITH ORGANOTIN COMPOUNDS

Kobayashi, Toshi-aki,Sakakura, Toshiyasu,Tanaka, Masato

, p. 3463 - 3466 (2007/10/02)

Imidoyl chlorides were successfully transformed into ketimines when treated with organotin compounds in the presence of palladium complex catalysts.

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