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304854-54-4

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304854-54-4 Usage

General Description

2-Amino-5-bromo-N-methoxy-N-methylbenzamide is a chemical compound with the molecular formula C9H10BrN2O2. It is a derivative of benzamide and contains an amino group, a bromine atom, and a methoxy group attached to the benzene ring. 2-Amino-5-bromo-N-methoxy-N-methylbenzamide has potential pharmaceutical applications, particularly in the development of new drugs. Its structure and properties make it a valuable building block in the synthesis of other organic compounds, and it may also exhibit biological activity that could be useful in medical research. The specific properties and potential uses of 2-Amino-5-bromo-N-methoxy-N-methylbenzamide make it a compound of interest for further study and application in the field of chemistry and pharmaceutical science.

Check Digit Verification of cas no

The CAS Registry Mumber 304854-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,8,5 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 304854-54:
(8*3)+(7*0)+(6*4)+(5*8)+(4*5)+(3*4)+(2*5)+(1*4)=134
134 % 10 = 4
So 304854-54-4 is a valid CAS Registry Number.

304854-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-5-bromo-N-methoxy-N-methylbenzamide

1.2 Other means of identification

Product number -
Other names 2-amino-5-bromo-N-methoxy-N-methyl-benzamide

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:304854-54-4 SDS

304854-54-4Relevant articles and documents

TEAD INHIBITORS AND USES THEREOF

-

Paragraph 00465; 00481, (2020/12/11)

The present invention provides compounds, compositions thereof, and methods of using the same.

Synthesis of Flubromazepam Positional Isomers for Forensic Analysis

Allred, B. McKay,France, Stefan,Jones, Lonnie V.,Ligon, Evelyn S.,Nawyn, Jason,Reinhardt, Daniel V.

, (2019/08/26)

Designer benzodiazepines have recently appeared in many forensic cases as legal alternatives to federally scheduled drugs such as diazepam (Valium) and alprazolam (Xanax). Though current forensic instrumental techniques are often sufficient for identifying novel psychoactive substances, they may not readily differentiate between potential positional isomers. Additionally, characterization data for positional isomers of known designer benzodiazepines are widely nonexistent. In this study, flubromazepam, a recognized designer benzodiazepine since 2012, was targeted for synthesis and characterization due to its potential for federal scheduling and current legal status within the United States. A practical synthetic method was developed to prepare purified reference materials for each positional isomer of flubromazepam in which the positions of the bromine and fluorine substituents were varied. Possible isomers (9 of the 12) were successfully prepared and used for further analysis.

Cascade Amination/Cyclization/Aromatization Process for the Rapid Construction of [2,3-c]Dihydrocarbazoles and [2,3-c]Carbazoles

Fan, Xing,Yu, Liu-Zhu,Wei, Yin,Shi, Min

supporting information, p. 4476 - 4479 (2017/09/11)

An intramolecular cascade amination/cyclization/aromatization reaction of functionalized alkylidenecyclopropanes has been developed in the presence of silver acetate, affording a variety of [2,3-c]dihydrocarbazoles and [2,3-c]carbazoles in moderate to excellent yields. The mechanistic investigations revealed that this cascade reaction proceeds through a radical initiated process. Moreover, further transformations for the synthesis of eustifoline-D and an OLED exhibit a potential synthetic utility of this method.

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