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N-(2-bromo-4,5-dimethoxyphenyl)acetamide is a chemical compound with the molecular formula C10H12BrNO3. It is a derivative of acetamide, featuring a 2-bromo-4,5-dimethoxyphenyl group attached to the nitrogen atom. N-(2-bromo-4,5-dimethoxyphenyl)acetamide is characterized by the presence of a bromine atom at the 2-position of the phenyl ring, and two methoxy groups at the 4 and 5 positions, respectively. The acetamide moiety provides a carboxamide functional group, which can participate in various chemical reactions and interactions. N-(2-bromo-4,5-dimethoxyphenyl)acetamide may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and reactivity.

5349-12-2

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5349-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5349-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5349-12:
(6*5)+(5*3)+(4*4)+(3*9)+(2*1)+(1*2)=92
92 % 10 = 2
So 5349-12-2 is a valid CAS Registry Number.

5349-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Brom-4-acetamino-veratrol

1.2 Other means of identification

Product number -
Other names acetic acid-(2-bromo-4,5-dimethoxy-anilide)

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:5349-12-2 SDS

5349-12-2Downstream Products

5349-12-2Relevant academic research and scientific papers

Site-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Amination

Baek, Junghyun,Ban, Jaeyoung,Lim, Minkyung,Rhee, Hakjune,Shabbir, Saira

, p. 917 - 927 (2020/03/13)

We synthesized various carbazoles from anilines through a three-step process with good overall yields (up to 48percent). This process comprises N -acetylation, copper(0)-mediated Ullmann homocoupling, and acid-mediated intramolecular amination. It permits various functional groups on the substrate. Scale-up of the developed three-step synthetic route to carbazoles was also demonstrated.

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