35691-93-1 Usage
Description
ETHYL 3,5-DIMETHYL-1H-4-PYRAZOLECARBOXYLATE, with the molecular formula C9H14N2O2, is an ester derivative of 3,5-dimethyl-1H-pyrazole-4-carboxylic acid. It is a yellow liquid with a slightly pungent odor, known for its flammable nature and potential hazards if ingested, inhaled, or absorbed through the skin. This chemical compound is predominantly utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, playing a crucial role in the development of various organic compounds.
Uses
Used in Pharmaceutical Industry:
ETHYL 3,5-DIMETHYL-1H-4-PYRAZOLECARBOXYLATE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, ETHYL 3,5-DIMETHYL-1H-4-PYRAZOLECARBOXYLATE is employed as an intermediate in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and management.
ETHYL 3,5-DIMETHYL-1H-4-PYRAZOLECARBOXYLATE is used as a chemical intermediate for the synthesis of various organic compounds due to its reactivity and functional group compatibility in chemical reactions, facilitating the creation of a wide range of products across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 35691-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,9 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35691-93:
(7*3)+(6*5)+(5*6)+(4*9)+(3*1)+(2*9)+(1*3)=141
141 % 10 = 1
So 35691-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2O2/c1-4-12-8(11)7-5(2)9-10-6(7)3/h4H2,1-3H3,(H,9,10)
35691-93-1Relevant articles and documents
Study of the Reaction of 2-(1-Alkoxyalkylidene)-1,3-dicarbonyl Compounds with Hydrazines
Emelina,Iz''yurov,Ermakov,Ershov
, p. 430 - 434 (2007/10/03)
13C NMR study has shown that the only site of primary attack by hydrazines on alkyl 3-oxobutanoates containing an alkoxymethylene or 1-alkoxyethylidene group in position 2 is the ethylenic carbon atom and that the corresponding enehydrazine is the only observable intermediate product. According to quantum-chemical calculations of the electronic structure of the substrates, the reaction is orbital-controlled.