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17072-38-7

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17072-38-7 Usage

Description

4-ethyl-1H-pyrazole is a pyrazole derivative with the molecular formula C5H8N2, known for its diverse biological activities and use as a building block in the synthesis of pharmaceuticals and agrochemicals.

Uses

Used in Pharmaceutical and Agrochemical Industries:
4-ethyl-1H-pyrazole is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used in Research Applications:
4-ethyl-1H-pyrazole is used as a ligand in coordination chemistry and as a reagent in organic synthesis, aiding in the advancement of scientific research and the discovery of new compounds.
It is important to handle 4-ethyl-1H-pyrazole with caution due to its potential hazards if not properly managed, and it exhibits moderate solubility in water and relative stability under standard conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 17072-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,7 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17072-38:
(7*1)+(6*7)+(5*0)+(4*7)+(3*2)+(2*3)+(1*8)=97
97 % 10 = 7
So 17072-38-7 is a valid CAS Registry Number.

17072-38-7 Well-known Company Product Price

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  • Aldrich

  • (CBR01738)  4-Ethyl-1H-pyrazole  AldrichCPR

  • 17072-38-7

  • CBR01738-1G

  • 5,476.77CNY

  • Detail

17072-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Ethyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole,4-ethyl

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:17072-38-7 SDS

17072-38-7Downstream Products

17072-38-7Relevant articles and documents

19-NOR C3,3-DISUBSTITUTED C21-N-PYRAZOLYL STEROIDS AND METHODS OF USE THEREOF

-

, (2014/11/11)

Provided herein are 19-nor C3,3-disubstituted C21-pyrazolyl steroids of Formula (I), and pharmaceutically acceptable salts thereof; wherein-, R1, R2, R3a, R3b, R4a, R4b, R5, R6, and R7are as defined herein. Such compounds are contemplated useful for the prevention and treatment of a variety of CNS-related conditions, for example, treatment of sleep disorders, mood disorders, schizophrenia spectrum disorders, convulsive disorders, disorders of memory and/or cognition, movement disorders, personality disorders, autism spectrum disorders, pain, traumatic brain injury, vascular diseases, substance abuse disorders and/or withdrawal syndromes, and tinnitus.

PURINE DERIVATIVES AS A2A RECEPTOR AGONISTS

-

, (2008/06/13)

A compound of formula (I) or stereoisomers or pharmaceutically acceptable salts thereof.and their preparation and use as A2A receptor agonists

Synthesis of the silver(I) complex of CH2[CH(pz 4Et)2]2 containing the unprecedented [Ag(NO3)4]3- anion: A general method for the preparation of 4-(alkyl)pyrazoles

Reger, Daniel L.,Gardinier, James R.,Grattan, T. Christian,Smith, Monica R.,Smith, Mark D.

, p. 1670 - 1677 (2007/10/03)

A general two-step method for the syntheses of 4-(alkyl)pyrazoles has been developed. The first step involves the reaction between organyl diethylacetals and the Vilsmeier reagent to give a mixture of ethoxy-and dimethylamino- acroleins. This mixture reacts directly with hydrazine monohydrogenchloride to yield the desired (4-substituted)pyrazoles. The 4-(phenyl)pyrazole derivative exhibited a markedly lower solubility in common organic solvents. In the solid state structure the phenyl and pyrazolyl groups are nearly coplanar and extensive intermolecular CH-π interactions organize the molecules in two-dimensional sheets that are held in a three dimensional arrangement by NH...N hydrogen bonds. Tetrakis[(4-ethyl)pyrazolyl]propane, CH 2[CH(pz4Et)2]2, was prepared by a transamination reaction and reacts with Ag(NO3) to yield a compound with a 4:3 metal:ligand mole ratio that when crystallized by diffusion of Et2O into an acetone solution produced [Ag2{μ-CH 2[CH(pz4Et)2]2}2] 3[Ag(NO3)4]2 (1). This complex contains dimeric units in which two silver cations are sandwiched between two CH2[CH(pz4Et)]2 ligands and the counterion is the unprecedented tetra(nitrato)argentate anion. ESI mass spectral data support the existence of both the cationic dimeric units and the [Ag(NO 3)4]- anion in solution.

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