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Methanone, (2-methoxy-5-nitrophenyl)phenyl-, also known as 1-(2-methoxy-5-nitrophenyl)ethanone, is an organic compound with the chemical formula C9H9NO4. It is a derivative of acetophenone, featuring a nitro group at the 5-position and a methoxy group at the 2-position on the phenyl ring. This yellow crystalline solid is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of dyes and pigments. The compound is known for its potential reactivity and should be handled with care due to its nitro group, which can pose safety and environmental concerns.

2750-15-4

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2750-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2750-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2750-15:
(6*2)+(5*7)+(4*5)+(3*0)+(2*1)+(1*5)=74
74 % 10 = 4
So 2750-15-4 is a valid CAS Registry Number.

2750-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methoxy-5-nitrophenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2-Methoxy-5-nitrobenzophenon

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:2750-15-4 SDS

2750-15-4Downstream Products

2750-15-4Relevant academic research and scientific papers

Decarboxylation with Carbon Monoxide: The Direct Conversion of Carboxylic Acids into Potent Acid Triflate Electrophiles

Kinney, R. Garrison,Arndtsen, Bruce A.

, p. 5085 - 5089 (2019)

We report a new strategy for the conversion of carboxylic acids into potent acid triflate electrophiles. The reaction involves oxidative carbonylation of carboxylic acids with I2 in the presence of AgOTf, and is postulated to proceed via acyl hypoiodites that react with CO to form acid triflates. Coupling this chemistry with subsequent trapping with arenes offers a mild, room temperature approach to generate ketones directly from broadly available carboxylic acids without the use of corrosive and reactive Lewis or Bronsted acid additives, and instead from compounds that are readily available, stable, and functional group compatible.

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