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115315-95-2

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115315-95-2 Usage

General Description

Ethyl 1-phenyl-1H-pyrazole-3-carboxylate, also known as ethyl phenylpyrazolyl acetate, is an organic compound that belongs to the class of pyrazole carboxylic acid esters. It is commonly used in the synthesis of pharmaceuticals and agrochemicals, as well as in the development of novel materials and chemical precursors. ethyl 1-phenyl-1H-pyrazole-3-carboxylate is a versatile building block in organic chemistry and is known for its role in the preparation of various biologically active molecules. It is often used as a reagent in organic synthesis and has the potential to be utilized in a wide range of applications in the field of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 115315-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,1 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115315-95:
(8*1)+(7*1)+(6*5)+(5*3)+(4*1)+(3*5)+(2*9)+(1*5)=102
102 % 10 = 2
So 115315-95-2 is a valid CAS Registry Number.

115315-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-phenylpyrazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 1-phenyl-1H-pyrazole-3-carboxylate

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:115315-95-2 SDS

115315-95-2Downstream Products

115315-95-2Relevant articles and documents

Haloacetylated enol ethers. 11 [16]. Synthesis of 1-methyl- and 1- phenyl pyrazole-3(5)-ethyl esters. A one-pot procedure

Martins, Marcos A. P.,Freitag, Rogerio A.,Da Rosa, Adriano,Flores, Alex F. C.,Zanatta, Nilo,Bonacorso, Helio G.

, p. 217 - 220 (1999)

A one-pot synthesis of 1-methyl- and 1-phenylpyrazole-3(5)-ethyl esters 2,3a-e by the cyclocondensation of β-alkoxyvinyl trichloromethyl ketones 1a- e with methyl and phenyl hydrazine hydrochloride under mild conditions, is reported. A study using compounds la-e with different substituents proved that these are versatile building blocks for the synthesis of pyrazole derivatives, having a 3(5)-ethoxycarbonyl substituent in good yields (60- 89%). The hydrazine and β-alkoxyvinyl trichloromethyl ketone substituent effects on the reaction regiochemistry on the formation of the 1,3- and 1,5- isomer were observed.

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