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Benzeneacetic acid, 5-bromo-2-nitro-, methyl ester is a chemical compound with the molecular formula C9H8BrNO4. It is a methyl ester of 5-bromo-2-nitrobenzeneacetic acid, characterized by its yellow to orange crystalline powder form. Benzeneacetic acid, 5-bromo-2-nitro-, methyl ester is commonly used in the synthesis of various pharmaceuticals and organic compounds, and is often utilized in research and development activities within the chemical and pharmaceutical industries.

189748-25-2

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189748-25-2 Usage

Uses

Used in Pharmaceutical Industry:
Benzeneacetic acid, 5-bromo-2-nitro-, methyl ester is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex organic molecules. Its unique structure allows it to be a key component in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, Benzeneacetic acid, 5-bromo-2-nitro-, methyl ester is used as a building block for the synthesis of a wide range of organic compounds. Its reactivity and functional groups make it a versatile component in creating new molecules with specific properties and applications.
It is important to handle and use Benzeneacetic acid, 5-bromo-2-nitro-, methyl ester with caution as it might pose potential health hazards if not properly handled and managed.

Check Digit Verification of cas no

The CAS Registry Mumber 189748-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,7,4 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 189748-25:
(8*1)+(7*8)+(6*9)+(5*7)+(4*4)+(3*8)+(2*2)+(1*5)=202
202 % 10 = 2
So 189748-25-2 is a valid CAS Registry Number.

189748-25-2SDS

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 methyl 2-(5-bromo-2-nitrophenyl)acetate

1.2 Other means of identification

Product number -
Other names methyl 2-(5-bromanyl-2-nitro-phenyl)ethanoate

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:189748-25-2 SDS

189748-25-2Downstream Products

189748-25-2Relevant academic research and scientific papers

Iron(II) bromide-catalyzed intramolecular c-h bond amination [1,2]-shift tandem reactions of aryl azides

Nguyen, Quyen,Nguyen, Tuyen,Driver, Tom G.

, p. 620 - 623 (2013/03/13)

Iron(II) bromide catalyzes the transformation of ortho-substituted aryl azides into 2,3-disubstituted indoles through a tandem ethereal C-H bond amination [1,2]-shift reaction. The preference for the 1,2-shift component of the tandem reaction was established to be Me 1 2 Ph.

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