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N-(2-methylpropyl)-3-nitrobenzamide is a chemical compound with the molecular formula C11H14N2O3. It is an amide derivative, characterized by the presence of a nitro group (-NO2) attached to the benzene ring at the 3rd position and an N-(2-methylpropyl) group (also known as an isobutyl group) attached to the nitrogen atom of the amide. N-(2-methylpropyl)-3-nitrobenzamide is often used in the synthesis of pharmaceuticals and agrochemicals due to its potential biological activity. Its structure allows for various functional group modifications, making it a versatile building block in organic chemistry.

2448-05-7

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2448-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2448-05-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2448-05:
(6*2)+(5*4)+(4*4)+(3*8)+(2*0)+(1*5)=77
77 % 10 = 7
So 2448-05-7 is a valid CAS Registry Number.

2448-05-7SDS

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 N-(2-methylpropyl)-3-nitrobenzamide

1.2 Other means of identification

Product number -
Other names 3-Nitro-benzoesaeure-isobutylamid

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:2448-05-7 SDS

2448-05-7Downstream Products

2448-05-7Relevant academic research and scientific papers

A Convenient One-Pot Synthesis of 1,5-Disubstituted Tetrazoles Containing an Amino or a Carboxy Group

Obushak, M. D.,Pokhodylo, N. T.,Shyyka, O. Ya.

, p. 802 - 812 (2020/07/03)

Abstract: A convenient method is proposed for constructing the tetrazole ring by a one-pot reaction of amides with phosphorus oxychloride and sodium azide. A series of 1,5-disubstituted tetrazoles containing an amino or a carboxy group, which present interest as buildings blocks for the synthesis of biologically active substances, were obtained.

Amidation and esterification of carboxylic acids with amines and phenols by N,N′-diisopropylcarbodiimide: A new approach for amide and ester bond formation in water

Fattahi, Nadia,Ayubi, Morteza,Ramazani, Ali

, p. 4351 - 4356 (2018/07/13)

The present study reports the successful synthesis of two important and abundant functional groups “ester and amide” by N,N′-diisopropylcarbodiimide (DIC) in water as a green solvent. A wide range of substrates could be employed with high functional group tolerance. The products were obtained in high yields after short reaction times. This method provides an efficient, economic, simple and very mild protocol for ester and amide bond formation in aqueous media. In addition, this work not only may lead to environmentally benign systems but also will provide a new aspect of organic chemistry in water.

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