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Methyl 3-[(2,4-dimethylphenyl)carbamoyl]-1H-pyrazole-1-carboxylate is a complex organic compound with the chemical formula C13H14N2O3. It is a derivative of pyrazole, a five-membered heterocyclic compound containing three nitrogen atoms. The molecule features a carbamoyl group (-CO-NH2) attached to the 3-position of the pyrazole ring, and a 2,4-dimethylphenyl group connected to the carbamoyl nitrogen. The compound is characterized by its methyl ester functionality, which is attached to the carboxylate group (-COO-) at the 1-position of the pyrazole ring. This chemical structure is relevant in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products.

6125-75-3

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6125-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6125-75-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6125-75:
(6*6)+(5*1)+(4*2)+(3*5)+(2*7)+(1*5)=83
83 % 10 = 3
So 6125-75-3 is a valid CAS Registry Number.

6125-75-3SDS

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 methyl 3-[(2,4-dimethylphenyl)carbamoyl]pyrazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names sec-butylidene-cyclohexyl-amine

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

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More Details:6125-75-3 SDS

6125-75-3Relevant academic research and scientific papers

HOMOLYTIC ADDITION OF 1,4-DIOXANE TO SCHIFF BASES

Pastushenko, E. V.,Safiulova, G. I.,Kruglov, D. E.

, p. 2143 - 2148 (2007/10/02)

Radical addition of 1,4-dioxane to aldimines proceeds at the imidyl carbon atom with formation of asymmetrical secondary amines.By the method of competitive kinetics we have determined the relative activities of Schiff bases and have found that the regiod

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