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Acetamide, 2-amino-N-(2-hydroxyethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75007-28-2

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75007-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75007-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,0 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75007-28:
(7*7)+(6*5)+(5*0)+(4*0)+(3*7)+(2*2)+(1*8)=112
112 % 10 = 2
So 75007-28-2 is a valid CAS Registry Number.

75007-28-2SDS

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 2-amino-N-(2-hydroxyethyl)acetamide

1.2 Other means of identification

Product number -
Other names 2-Glycylamino-aethanol

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:75007-28-2 SDS

75007-28-2Relevant academic research and scientific papers

Selective oxidation of monoethanolamine to glycine over supported gold catalysts: The influence of support and the promoting effect of polyvinyl alcohol

Meng, Xiangzhan,Bai, Yinge,Xu, Haiyang,Zhang, Yongqiang,Li, Chunshan,Wang, Hui,Li, Zengxi

, p. 131 - 143 (2019/03/26)

Glycine is an important fine chemical used in many fields, and the traditional synthetic methods like Strecker synthesis and ammoniation of chloroacetic acid use highly toxic reagents or produce equal molar byproducts. Herein, selective aerobic oxidation of monoethanolamine (MEA) to glycine using Au catalysts supported on various supports, including Al2O3, SiO2, TiO2, ZnO, and ZrO2, was investigated and the correlation between acid-base properties of the catalysts and catalytic performance was established. Catalysts with higher base content exhibited higher initial activity and that with lower acid content gave higher glycine selectivity. The influence of preparation methods was revealed using Au/ZrO2 with the best catalytic performance and it was demonstrated that the presence of polyvinyl alcohol (PVA) has a significant promoting effect. In-situ FTIR and 1H NMR analysis revealed that the hydrogen bonds between PVA and MEA can enhance adsorption of MEA on catalysts, resulting in doubled turnover frequency (TOF) and improved MEA conversion; and the preferential hydrogen bonds between the amino group of MEA and the hydroxyl of PVA can prevent the coordination of amino group with Au nanoparticles, favoring reaction of the hydroxyl group of MEA on the active sites, accounting for the enhanced glycine selectivity. The reaction conditions were optimized and the optimal yield of glycine was 95%.

RUTHENIUM COMPLEXES AND THEIR USES AS CATALYSTS IN PROCESSES FOR FORMATION AND/OR HYDROGENATION OF ESTERS, AMIDES AND RELATED REACTIONS

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Paragraph 0281; 0325, (2017/10/18)

The present invention relates to novel Ruthenium complexes of formulae A1-A4 and their use, inter alia, for (1) dehydrogenative coupling of alcohols to esters; (2) hydrogenation of esters to alcohols (including hydrogenation of cyclic esters (lactones) or cyclic di-esters (di-lactones), or polyesters); (3) preparing amides from alcohols and amines—(including the preparation of polyamides (e.g., polypeptides) by reacting dialcohols and diamines and/or polymerization of amino alcohols and/or forming cyclic dipeptides from p-aminoalcohols; (4) hydrogenation of amides (including cyclic dipeptides, polypeptides and polyamides) to alcohols and amines; (5) hydrogenation of organic carbonates (including polycarbonates) to alcohols or hydrogenation of carbamates (including polycarbamates) or urea derivatives to alcohols and amines; (6) dehydrogenation of secondary alcohols to ketones; (7) amidation of esters (i.e., synthesis of amides from esters and amines); (8) acylation of alcohols using esters; (9) coupling of alcohols with water and a base to form carboxylic acids; and (10) preparation of amino acids or their salts by coupling of amino alcohols with water and a base. The present, invention further relates to the use of certain known Ruthenium complexes for the preparation of amino acids or their salts from amino alcohols.

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