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103440-95-5

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103440-95-5 Usage

General Description

4-Ethyl-3-nitrobenzoic acid is an organic compound that falls under the category of benzoic acids. It is primarily recognized for its core structural components, which comprises a nitro group (-NO2) and an ethyl group (-C2H5), attached to a benzoic acid framework. The presence of the nitro group enhances the compound's reactivity, making it valuable in the synthesis of various organic substances. It is characterized by the molecular formula C9H9NO4. Like other benzoic acids, 4-ethyl-3-nitrobenzoic acid exhibits carboxylic acid functionality, known for producing a sour taste and reacting with bases and carbonates to form salts. Due to its reactivity, this compound is often used in the manufacturing of dyes, pharmaceuticals, and resins. It can also be used as a precursor for the synthesis of other chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 103440-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,4 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103440-95:
(8*1)+(7*0)+(6*3)+(5*4)+(4*4)+(3*0)+(2*9)+(1*5)=85
85 % 10 = 5
So 103440-95-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c1-2-6-3-4-7(9(11)12)5-8(6)10(13)14/h3-5H,2H2,1H3,(H,11,12)

103440-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Ethyl-3-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-ETHYL-3-NITROBENZOIC 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:103440-95-5 SDS

103440-95-5Relevant articles and documents

Ionic tags for synthesis of oligoribonucleotides

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Page/Page column 61-62; 115-117; 155-157, (2018/04/12)

The invention relates to the chemical synthesis of oligonucleotides, e.g., oligoribonucleotides. In another aspect, the invention relates to compounds of formula (II) processes for making these compounds, and the use thereof in the chemical synthesis of o

Synthetic, structural mimetics of the β-hairpin flap of HIV-1 protease inhibit enzyme function

Chauhan, Jay,Chen, Shen-En,Fenstermacher, Katherine J.,Naser-Tavakolian, Aurash,Reingewertz, Tali,Salmo, Rosene,Lee, Christian,Williams, Emori,Raje, Mithun,Sundberg, Eric,Destefano, Jeffrey J.,Freire, Ernesto,Fletcher, Steven

, p. 7095 - 7109 (2015/11/11)

Small-molecule mimetics of the β-hairpin flap of HIV-1 protease (HIV-1 PR) were designed based on a 1,4-benzodiazepine scaffold as a strategy to interfere with the flap-flap protein-protein interaction, which functions as a gated mechanism to control acce

GPR40 RECEPTOR AGONIST, METHODS OF PREPARING THE SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AS AN ACTIVE INGREDIENT

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Paragraph 1151-1154, (2014/05/24)

The present invention relates to a novel compound having GPR40 receptor agonist activity that promotes insulin secretion and inhibits blood sugar rise after glucose loading, and is thereby useful for the treatment of diabetes and complications thereof, the preparation method thereof and pharmaceutical composition containing them as an active ingredient.

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