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3,4,5-triethoxy-N-(4-ethoxy-2-nitrophenyl)benzamide is a complex organic chemical compound with the molecular formula C20H24N2O8. It is characterized by the presence of three ethoxy groups attached to the benzene ring, a nitro group on the phenyl ring, and an amide functional group. 3,4,5-triethoxy-N-(4-ethoxy-2-nitrophenyl)benzamide is a derivative of benzamide, which is known for its potential applications in pharmaceuticals and agrochemicals. The specific arrangement of functional groups in 3,4,5-triethoxy-N-(4-ethoxy-2-nitrophenyl)benzamide may influence its chemical reactivity and physical properties, making it a subject of interest for researchers in the field of organic chemistry.

5700-61-8

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5700-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5700-61-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5700-61:
(6*5)+(5*7)+(4*0)+(3*0)+(2*6)+(1*1)=78
78 % 10 = 8
So 5700-61-8 is a valid CAS Registry Number.

5700-61-8SDS

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 3,4,5-triethoxy-N-(4-ethoxy-2-nitrophenyl)benzamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5700-61-8 SDS

5700-61-8Relevant academic research and scientific papers

Copper-Catalyzed Propargylation of Nitroalkanes

Kim, Raphael S.,Dinh-Nguyen, Linh V.,Shimkin, Kirk W.,Watson, Donald A.

supporting information, p. 8106 - 8110 (2020/11/02)

Using a commercially available, inexpensive, and abundant copper catalyst system, an efficient α-functionalization of nitroalkanes with propargyl bromides is now established. This mild and robust method is highly functional group tolerant and provides straightforward access to complex secondary and tertiary homopropargylic nitroalkanes. Moreover, the utility of these α-propargylated nitroalkanes is demonstrated through downstream functionalization to biologically relevant, five-membered N-heterocycles such as pyrroles and 2-pyrrolines.

Copper diamine complexes and their use as bleach activating catalysts

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Page/Page column 6-7, (2008/06/13)

Bleach activators are herein disclosed having the stoichiometric formula: wherein R1, R2, R3, R4, R5 and R6 are each a radical selected from the group consisting of hydrogen, alkyl, aryl, alkylaryl, arylalkyl, phenyl, benzyl and mixtures thereof, or R5 and R6 together form a hydrogen carbon ring, n is an integer from 0 to 1, m is an integer from 1 to 2, and X is selected from mono- and polyvalent anions. These bleach activators are combined with a peroxygen compound capable of releasing hydrogen perioxide in an aqueous solution. The combination is especially effective in the removal of hydrophobic stains from fabrics.

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