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5433-09-0

3-(benzoylamino)propyl benzoate is a chemical compound with the molecular formula C17H15NO3. It is an ester derivative of benzoic acid, where the hydroxyl group of benzoic acid is replaced by a 3-(benzoylamino)propyl group. 3-(benzoylamino)propyl benzoate is characterized by its aromatic structure, featuring two benzene rings connected through an amide linkage. It is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique chemical properties. The compound's structure allows for interactions with other molecules, making it a subject of interest for researchers exploring its possible uses and effects.

5433-09-0

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5433-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5433-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5433-09:
(6*5)+(5*4)+(4*3)+(3*3)+(2*0)+(1*9)=80
80 % 10 = 0
So 5433-09-0 is a valid CAS Registry Number.

5433-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzamidopropyl benzoate

1.2 Other means of identification

Product number -
Other names 3-Benzamidopropyl-benzoat

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:5433-09-0 SDS

5433-09-0Downstream Products

5433-09-0Relevant articles and documents

Microwave-Promoted Transformations: Fast and Chemoselective N-Acylation of Amino Alcohols Using Catalytic Amounts of Dibutyltin Oxide. Influence of the Power Output and the Nature of the Acylating Agent on the Selectivity

Morcuende, Anabel,Ors, Marta,Valverde, Serafin,Herradon, Berbardo

, p. 5264 - 5270 (2007/10/03)

The influence of the nature of the acylating agent and the power output on the chemoselectivity of the microwave-mediated acylation of 1,2- and 1,3-amino alcohols catalyzed by dibutyltin oxide has been studied.The method constitutes an efficient procedure for the selective N-acylation of amino alcohols.

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