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2-[ACETYL(METHYL)AMINO]BENZOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78944-67-9

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78944-67-9 Usage

General Description

2-[Acetyl(methyl)amino]benzoic acid is a chemical compound with the molecular formula C10H11NO3. It is a derivative of benzoic acid with an acetyl(methyl)amino group attached to the 2-position. 2-[ACETYL(METHYL)AMINO]BENZOIC ACID is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs. It has analgesic and anti-inflammatory properties, and is often used in the production of nonsteroidal anti-inflammatory drugs (NSAIDs). Additionally, 2-[Acetyl(methyl)amino]benzoic acid has also been studied for its potential use in the treatment of cancer due to its ability to inhibit the growth of tumor cells. Overall, 2-[ACETYL(METHYL)AMINO]BENZOIC ACID has several important applications in both the pharmaceutical and medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 78944-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,4 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78944-67:
(7*7)+(6*8)+(5*9)+(4*4)+(3*4)+(2*6)+(1*7)=189
189 % 10 = 9
So 78944-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-7(12)11(2)9-6-4-3-5-8(9)10(13)14/h3-6H,1-2H3,(H,13,14)

78944-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[Acetyl(methyl)amino]benzoic acid

1.2 Other means of identification

Product number -
Other names N-Acetyl-N-methyl-anthranilsaeure

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:78944-67-9 SDS

78944-67-9Downstream Products

78944-67-9Relevant academic research and scientific papers

Oxidative Cleavage of Indoles Mediated by Urea Hydrogen Peroxide or H2O2 in Polar Solvents

Llopis, Natalia,Gisbert, Patricia,Baeza, Alejandro

supporting information, p. 3245 - 3249 (2021/06/08)

The oxidative cleavage of indoles (Witkop oxidation) involving the use of H2O2 or urea hydrogen peroxide in combination with a polar solvent has been described. Among these solvents, 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) stands out as the one affording the corresponding 2-ketoacetanilides generally in higher yields The protocol described has also enabled the oxidation of different pyrroles and furans derivatives. Furthermore, the procedure was implemented in a larger-scale and HFIP was distilled from the reaction mixture and reused (up to 4 cycles) without a significant detriment in the reaction outcome, which remarks its sustainability and applicability. (Figure presented.).

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