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N-(4-ethoxyphenyl)-3,4,5-trimethoxybenzamide is a complex organic compound with the molecular formula C18H21NO5. It is characterized by a benzamide structure, where the benzene ring is substituted with three methoxy groups at the 3, 4, and 5 positions, and an ethoxyphenyl group is attached to the nitrogen atom. N-(4-ethoxyphenyl)-3,4,5-trimethoxybenzamide is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting various biological pathways. Its chemical structure endows it with specific properties that make it a subject of interest for scientists exploring new therapeutic agents.

4043-16-7

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4043-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4043-16-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4043-16:
(6*4)+(5*0)+(4*4)+(3*3)+(2*1)+(1*6)=57
57 % 10 = 7
So 4043-16-7 is a valid CAS Registry Number.

4043-16-7SDS

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 1,1'-Biphenyl,3,4,5-tribromo

1.2 Other means of identification

Product number -
Other names 3,4,5-tribromo-biphenyl

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:4043-16-7 SDS

4043-16-7Downstream Products

4043-16-7Relevant academic research and scientific papers

Synthesis and CNS-depressant profile of 3,4,5-trimethoxybenzoyl analogues

Kar

, p. 313 - 315 (2007/10/02)

A series of 3,4,5-trimethoxybenzoyl analogues with varying electronic and stereochemical characteristics has been synthesized. Many of these compounds (4, 5, 9, 12, 15) showed appreciable potentiation of pentobarbitone-induced hypnosis. Several analogues (1, 5, 6, 11, 12, 15) exhibited marked reduction of spontaneous motor activity (SMA).

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