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3-Bromo-4-methoxyphenylacetic acid, a brominated derivative of 4-methoxyphenylacetic acid, is a chemical compound with the molecular formula C9H9BrO3. It features a bromine atom substituted at the third carbon position, making it a valuable building block in organic synthesis and medicinal chemistry for the creation of pharmaceuticals and biologically active molecules. 3-BROMO-4-METHOXYPHENYLACETIC ACID has garnered interest due to its potential anti-inflammatory and analgesic properties, as well as its role in the development of new drugs. Additionally, it serves as a reagent for the preparation of esters, amides, and other organic compounds.

774-81-2

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774-81-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-4-methoxyphenylacetic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs with anti-inflammatory and analgesic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 3-Bromo-4-methoxyphenylacetic acid is utilized as a building block for creating a range of biologically active molecules, highlighting its versatility in chemical reactions.
Used as a Reagent:
3-Bromo-4-methoxyphenylacetic acid is employed as a reagent in the preparation of esters, amides, and other organic compounds, facilitating the synthesis of a diverse array of chemical entities for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 774-81-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 774-81:
(5*7)+(4*7)+(3*4)+(2*8)+(1*1)=92
92 % 10 = 2
So 774-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO3/c1-13-8-3-2-6(4-7(8)10)5-9(11)12/h2-4H,5H2,1H3,(H,11,12)

774-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Bromo-4-methoxyphenyl)acetic Acid

1.2 Other means of identification

Product number -
Other names 2-(3-bromo-4-methoxyphenyl)acetic acid

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:774-81-2 SDS

774-81-2Relevant academic research and scientific papers

Novel dihydroquinolizinones for the treatment and prophylaxis of hepatitis B virus infection

-

, (2015/08/04)

The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds.

NOVEL DIHYDROQUINOLIZINONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

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, (2015/09/23)

The invention provides novel compounds having the general formula (I) wherein R1, R2 R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds in the treatment of the hepatitis B virus.

PHENYL-ALKYL PIPERAZINES HAVING TNF-MODULATING ACTIVITY, PREPARATION METHOD, AND THERAPEUTIC USE THEREOF

-

Page/Page column 5, (2011/06/26)

The present invention relates to phenyl-alkyl piperazines of formula (I): in which A, R1, R2 and R3 are as defined herein, having TNF-modulating activity. The invention also relates to the preparation thereof, pharmaceutical compositions thereof, and to t

2- [5- (5-carbamimidoyl-1H-heteroaryl)-6-hydroxybiphenyl-3-yl]-succinic acid derivatives as factor viia inhibitors

-

, (2008/06/13)

The present invention relates to novel inhibitors of Factors VIIa, IXa, Xa, XIa, in particular Factor VIIa, pharmaceutical compositions comprising these inhibitors, and methods for using these inhibitors for treating or preventing thromboembolic disorders. Processes for preparing these inhibitors are also disclosed.

Syntheses of the marine metabolites verongamine, hemibastadin-2, and aerothionin using the cyano ylide coupling methodology

Wasserman, Harry H.,Wang, Jianji

, p. 5581 - 5586 (2007/10/03)

Syntheses of the marine metabolites verongamine, hemibastadin-2, and aerothionin have been accomplished by a methodology involving the conversion of a carboxylic acid to an acyl cyano phosphorane which may be oxidized to an α,β-diketo nitrile. This strong

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