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92939-26-9

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92939-26-9 Usage

General Description

1H-Pyrazole-3-carboxylic acid, 4-propyl-, ethyl ester is a chemical compound with the molecular formula C10H14N2O2. It is an ester derivative of pyrazole carboxylic acid, and it is commonly used as an intermediate in the synthesis of pharmaceutical compounds and agrochemicals. This chemical has various potential applications due to its structural properties and ability to participate in different chemical reactions. It is important to handle and store this compound with care, as it may pose health and environmental hazards if not managed properly. Overall, 1H-Pyrazole-3-carboxylic acid, 4-propyl-, ethyl ester is a versatile chemical that has a broad range of potential uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 92939-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,3 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92939-26:
(7*9)+(6*2)+(5*9)+(4*3)+(3*9)+(2*2)+(1*6)=169
169 % 10 = 9
So 92939-26-9 is a valid CAS Registry Number.

92939-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-propyl-1H-pyrazole-3-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 1H-PYRAZOLE-3-CARBOXYLIC ACID, 4-PROPYL-, 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:92939-26-9 SDS

92939-26-9Upstream product

92939-26-9Relevant articles and documents

Preparations of 4-substituted 3-carboxypyrazoles

Janin, Yves L.

, p. 1410 - 1414 (2014/01/06)

The scopes of three synthetic methods reported for the preparation of an array of 3-pyrazolecarboxylates featuring substituents on position 4 were investigated. The first one is based on the potassium permanganate oxidation of methylpyrazoles. The second starts with the condensation between DMF dimethylacetal and ethyl pyruvate and is followed by the addition of hydrazine hydrochloride. The last one makes use of the cycloaddition of diazomethane on acrylate esters followed by a bromine-based oxidative rearrangement into 4-substituted 3-pyrazole esters.

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