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122898-67-3

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122898-67-3 Usage

Uses

dyspepsia therapy

Check Digit Verification of cas no

The CAS Registry Mumber 122898-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 122898-67:
(8*1)+(7*2)+(6*2)+(5*8)+(4*9)+(3*8)+(2*6)+(1*7)=153
153 % 10 = 3
So 122898-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H26N2O4/c1-22(2)11-12-26-17-8-5-15(6-9-17)14-21-20(23)16-7-10-18(24-3)19(13-16)25-4/h5-10,13H,11-12,14H2,1-4H3,(H,21,23)

122898-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[4-[2-(dimethylamino)ethoxy]phenyl]methyl]-3,4-dimethoxybenzamide

1.2 Other means of identification

Product number -
Other names Itopride (INN)

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:122898-67-3 SDS

122898-67-3Relevant articles and documents

Generation of Oxyphosphonium Ions by Photoredox/Cobaloxime Catalysis for Scalable Amide and Peptide Synthesis in Batch and Continuous-Flow

Chen, Xiangyang,Houk, Kendall N.,Mo, Jia-Nan,Su, Junqi,Umanzor, Alexander,Zhang, Zheng,Zhao, Jiannan

supporting information, (2022/01/06)

Phosphine-mediated deoxygenative nucleophilic substitutions, such as the Mitsunobu reaction, are of great importance in organic synthesis. However, the conventional protocols require stoichiometric oxidants to trigger the formation of the oxyphosphonium i

Manganese Catalyzed Direct Amidation of Esters with Amines

Fu, Zhengqiang,Wang, Xinghua,Tao, Sheng,Bu, Qingqing,Wei, Donghui,Liu, Ning

, p. 2339 - 2358 (2021/02/03)

The transition metal catalyzed amide bond forming reaction of esters with amines has been developed as an advanced approach for overcoming the shortcomings of traditional methods. The broad scope of substrates in transition metal catalyzed amidations remains a challenge. Here, a manganese(I)-catalyzed method for the direct synthesis of amides from a various number of esters and amines is reported with unprecedented substrate scope using a low catalyst loading. A wide range of aromatic, aliphatic, and heterocyclic esters, even in fatty acid esters, reacted with a diverse range of primary aryl amines, primary alkyl amines, and secondary alkyl amines to form amides. It is noteworthy that this approach provides the first example of the transition metal catalyzed amide bond forming reaction from fatty acid esters and amines. The acid-base mechanism for the manganese(I)-catalyzed direct amidation of esters with amines was elucidated by DFT calculations.

method for preparing itopride using micro flow reactor

-

Paragraph 0023; 0058-0067, (2018/05/26)

The present invention relates to a method for preparing itopride by using a micro flow reactor, wherein the yield and the degree of purity of the itopride generated by using the micro flow reactor can be improved; thionyl chloride or oxalyl chloride can be safely used; and leakage of noxious gases, such as a sulfur dioxide gas and/or a hydrochloric acid gas can be prevented. Also, the itopride can be manufactured through a simple process without an extra separation and purification process of an intermediate product that is generated during manufacturing.

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