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N-(3-bromophenyl)-2-methoxyacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

430463-83-5

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430463-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 430463-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,0,4,6 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 430463-83:
(8*4)+(7*3)+(6*0)+(5*4)+(4*6)+(3*3)+(2*8)+(1*3)=125
125 % 10 = 5
So 430463-83-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H10BrNO2/c1-13-6-9(12)11-8-4-2-3-7(10)5-8/h2-5H,6H2,1H3,(H,11,12)

430463-83-5SDS

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 N-(3-bromophenyl)-2-methoxyacetamide

1.2 Other means of identification

Product number -
Other names HMS2359I05

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:430463-83-5 SDS

430463-83-5Downstream Products

430463-83-5Relevant academic research and scientific papers

COUMARIN-LIKE CYCLIC COMPOUND AS MEK INHIBITOR AND USE THEREOF

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Paragraph 0159-0161, (2020/05/30)

Disclosed are a class of coumarin-like cyclic compounds as MEK inhibitors and pharmaceutical compositions comprising the compounds, and the use of same in the preparation of a drug for treating MEK-related diseases. Particularly disclosed are compounds as shown in formula (I) and pharmaceutically acceptable salts thereof or tautomers thereof.

HETEROARYL COMPOUNDS AND PHARMACEUTICAL APPLICATIONS THEREOF

-

, (2016/01/25)

The present invention provides herein is a heteroaryl compound or a stereoisomer, a geometric isomer, a tautomer, a racemate, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof, as well as a pharmaceutical composition containing the compound disclosed herein. The present invention also provides herein is use of the compound or the pharmaceutical composition thereof disclosed herein in the manufacture of a medicine for treating autoimmune diseases or proliferative diseases.

Palladium-catalyzed anilide ortho-arylation and subsequent one-pot cyclization to phenanthridines

Shabashov, Dmitry,Daugulis, Olafs

, p. 7720 - 7725 (2008/02/12)

(Chemical Equation Presented) The palladium-catalyzed direct arylation of anilides possessing several N-acyl substituents has been demonstrated. Removal of the acyl group by base hydrolysis allows a short and efficient synthesis of 2-aryl or 2,6-diarylanilines. The method is functional group tolerant and allows the presence of chloride and bromide substituents on both the anilide and aryl iodide coupling components. The arylation products can be converted to phenanthridines by the reaction with trifluoroacetic anhydride.

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