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39796-49-1

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39796-49-1 Usage

General Description

2-Benzylaminoacetamide is a chemical compound with the molecular formula C10H13N3O. It is a derivative of acetamide with a benzylamine group attached to the nitrogen atom. 2-Benzylaminoacetamide has been studied for its potential pharmaceutical properties and is known to exhibit anti-inflammatory and antimicrobial activities. It has also been investigated for its potential use as a building block in organic synthesis. 2-Benzylaminoacetamide shows promise as a versatile starting material for the synthesis of various biologically active molecules and may have potential applications in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 39796-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,9 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39796-49:
(7*3)+(6*9)+(5*7)+(4*9)+(3*6)+(2*4)+(1*9)=181
181 % 10 = 1
So 39796-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O/c10-9(12)7-11-6-8-4-2-1-3-5-8/h1-5,11H,6-7H2,(H2,10,12)

39796-49-1SDS

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-(benzylamino)acetamide

1.2 Other means of identification

Product number -
Other names N-Benzyl-glycin-amid

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:39796-49-1 SDS

39796-49-1Relevant articles and documents

Carbohydrates as efficient catalysts for the hydration of α-amino nitriles

Chitale, Sampada,Derasp, Joshua S.,Hussain, Bashir,Tanveer, Kashif,Beauchemin, André M.

supporting information, p. 13147 - 13150 (2016/11/09)

Directed hydration of α-amino nitriles was achieved under mild conditions using simple carbohydrates as catalysts exploiting temporary intramolecularity. A broadly applicable procedure using both formaldehyde and NaOH as catalysts efficiently hydrated a variety of primary and secondary susbtrates, and allowed the hydration of enantiopure substrates to proceed without racemization. This work also provides a rare comparison of the catalytic activity of carbohydrates, and shows that the simple aldehydes at the basis of chemical evolution are efficient organocatalysts mimicking the function of hydratase enzymes. Optimal catalytic efficiency was observed with destabilized aldehydes, and with difficult substrates only simple carbohydrates such as formaldehyde and glycolaldehyde proved reliable.

SUBSTITUTED (THIOPHENYL-CARBONYL)IMIDAZOLIDINONES, AND USE THEREOF

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Page/Page column 11, (2012/02/03)

The present invention relates to novel substituted (thiophenyl-carbonyl)imidazolidinones, methods for their production, their use for the treatment and/or prevention of diseases, as well as their use for the production of medicaments for the treatment and/or prophylaxis of diseases, especially retroviral diseases, in humans and/or animals.

SUBSTITUTED (PYRAZOLYLCARBONYL)IMIDAZOLIDINONES AND THEIR USE

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Page/Page column 38, (2011/06/19)

The present invention relates to novel substituted (pyrazolylcarbonyl)imidazolidinones, methods for their preparation, their use for the treatment and/or prophylaxis of diseases, as well as their use for the manufacture of medicaments for the treatment and/or prophylaxis of diseases, especially of retroviral diseases, in humans and/or animals.

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