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Propanamide, N-butyl-2-oxo- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98435-83-7

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98435-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98435-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,3 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 98435-83:
(7*9)+(6*8)+(5*4)+(4*3)+(3*5)+(2*8)+(1*3)=177
177 % 10 = 7
So 98435-83-7 is a valid CAS Registry Number.

98435-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-1,2-dioxopropylamine

1.2 Other means of identification

Product number -
Other names Brenztraubensaeure-butylamid

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:98435-83-7 SDS

98435-83-7Relevant academic research and scientific papers

Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles

Wang, Dong,Li, Linna,Feng, Hairong,Sun, Hua,Almeida-Veloso, Fabrice,Charavin, Marine,Yu, Peng,Désaubry, Laurent

supporting information, p. 2775 - 2780 (2018/06/27)

An efficient synthesis of fully substituted 2,3-dihydropyrroles has been achieved in one step through the three-component reaction of amines, aromatic aldehydes and α-ketoamides. This atom-economical and catalyst-free reaction is highly stereoselective and generates underexplored heterocycles in a single step. These compounds were examined in an enzymatic assay that led to the identification of potent α-glucosidase inhibitors, thereby demonstrating the utility of this novel methodology in medicinal chemistry.

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