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N-Acetoacetyl cresidine is a chemical compound characterized by its yellow to dark brown powder form, with a molecular formula of C11H12N2O2 and a molecular weight of 204.23 g/mol. It is synthesized through the condensation of acetoacetic acid with 2-amino-4-methylphenol, followed by acetylation of the resulting product. N-Acetoacetyl cresidine serves as a diazo coupling component in the production of azo dyes and is also utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. However, due to potential health hazards associated with inhalation, ingestion, or skin contact, handling N-Acetoacetyl cresidine requires appropriate safety measures.

85968-72-5

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85968-72-5 Usage

Uses

Used in Dye Industry:
N-Acetoacetyl cresidine is used as a diazo coupling component for the production of azo dyes, which are widely used in various applications such as coloring textiles, plastics, and paints due to their vibrant color properties and stability.
Used in Pharmaceutical and Agrochemical Industries:
N-Acetoacetyl cresidine is utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products that can improve human health and crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 85968-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,6 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85968-72:
(7*8)+(6*5)+(5*9)+(4*6)+(3*8)+(2*7)+(1*2)=195
195 % 10 = 5
So 85968-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO3/c1-8-4-5-11(16-3)10(6-8)13-12(15)7-9(2)14/h4-6H,7H2,1-3H3,(H,13,15)

85968-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Acetoacetyl cresidine

1.2 Other means of identification

Product number -
Other names 5'-Methyl-o-acetoacetanisidide

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:85968-72-5 SDS

85968-72-5Relevant academic research and scientific papers

Knorr cyclizations and distonic superelectrophiles

Sai, Kiran Kumar Solingapuram,Gilbert, Thomas M.,Klumpp, Douglas A.

, p. 9761 - 9764 (2008/03/27)

(Chemical Equation Presented) The acid-catalyzed Knorr cyclization has been studied by experimental and theoretical methods. The results of these studies indicate that β-ketoamides such as acetoacetanilide undergo diprotonation at the two carbonyl oxygen atoms to form distonic superelectrophiles. Direct observation of a dicationic superelectrophile was achieved by low-temperature 1H, 15N, and 13C NMR from FSO 3H-SbF5-SO2ClF solutions. In synthetic studies, the Bronsted superacid CF3SO3H is found to be an effective acid catalyst for the Knorr cyclization.

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