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187159-25-7

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187159-25-7 Usage

General Description

1H-Pyrazole-3-carboxylic acid, 4-(4-Methylphenyl)-, ethyl ester is a chemical compound with the molecular formula C14H14N2O2. It is an ethyl ester derivative of 1H-pyrazole-3-carboxylic acid, and contains a 4-(4-Methylphenyl) substituent. 1H-Pyrazole-3-carboxylic acid, 4-(4-Methylphenyl)-, ethyl ester is used as a building block in organic synthesis and medicinal chemistry, and has potential applications in the pharmaceutical industry. It may be used as a precursor in the synthesis of other compounds, and its properties and potential biological activity make it a subject of interest for scientific research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 187159-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,1,5 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 187159-25:
(8*1)+(7*8)+(6*7)+(5*1)+(4*5)+(3*9)+(2*2)+(1*5)=167
167 % 10 = 7
So 187159-25-7 is a valid CAS Registry Number.

187159-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-p-Tolyl-2H-pyrazole-3-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 1H-PYRAZOLE-3-CARBOXYLIC ACID, 4-(4-METHYLPHENYL)-, ETHYL ESTER

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:187159-25-7 SDS

187159-25-7Downstream Products

187159-25-7Relevant articles and documents

Synthesis and reactions of some ethyl 3-aroyl-4-aryl-2-pyrazoline-5-carboxylates

Faidallah,Makki,Elmassry,Hassan

, p. 101 - 105 (2007/10/03)

A series of ethyl 3-aroyl-4-aryl-2-pyrazoline-5-carboxylates 1 was prepared. Their reactions with bromine water, potassium permanganate and potassium hydroxide afforded the corresponding pyrazoles. With aryl and aroyl hydrazines the pyrazolines 1 gave the Schiff bases 9 while with hydrazine hydrate they yielded the corresponding acid hydrazides 11. Condensation of 11 with aromatic aldehydes gave the arylidene derivatives 12, which on cyclization with the proper reagent afforded 13 or 14. Reaction of 1 with hydrochloric acid gave the corresponding dipyrazolo-pyrazine derivatives 10.

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