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4-ethoxy-3-nitro-N-[4-(propanoylamino)phenyl]benzamide is a complex organic compound with the molecular formula C18H20N4O5. It is a derivative of benzamide, featuring a nitro group at the 3-position, an ethoxy group at the 4-position, and a propanoylamino group attached to the 4-position of the phenyl ring. 4-ethoxy-3-nitro-N-[4-(propanoylamino)phenyl]benzamide is characterized by its potential pharmaceutical applications, as it belongs to a class of compounds that can exhibit biological activity. Its structure suggests that it may be involved in various chemical reactions and could be a precursor in the synthesis of other pharmaceutically relevant molecules. The compound's specific properties, such as solubility and stability, would depend on the conditions under which it is stored and used.

5838-79-9

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5838-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5838-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5838-79:
(6*5)+(5*8)+(4*3)+(3*8)+(2*7)+(1*9)=129
129 % 10 = 9
So 5838-79-9 is a valid CAS Registry Number.

5838-79-9SDS

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 4-ethoxy-3-nitro-N-[4-(propanoylamino)phenyl]benzamide

1.2 Other means of identification

Product number -
Other names 2,2-Dibenzyl-1,3-thioxane

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:5838-79-9 SDS

5838-79-9Relevant academic research and scientific papers

A Selectivity Study of Activated Ketal Reduction with Borane Dimethyl Sulfide

Bartels, Birgit,Hunter, Roger

, p. 6756 - 6765 (2007/10/02)

A chemo- and regioselectivity study of the reagent combination BH3*SMe2/TMSOTf for ketal reduction has been undertaken.It has revealed that simple 1,3-dioxanes reduce cleanly at low temperature in CH2Cl2 while simple 1,3-dioxolanes may give complete ring cleavage and dimerization products.A study of reduction of 4-substituted 1,3-dioxolanes has revealed a solvent-directed regioselectivity which in THF favors the secondary protected derivative.A mechanism is postulated to account for the selectivities based on recent thinking on acetal substitution reactions.

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