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3,5-Dimethyl-1H-pyrazol-4-ol is an organic compound with the molecular formula C5H8N2O. It is a heterocyclic molecule, specifically a pyrazole derivative, characterized by the presence of two nitrogen atoms in a five-membered ring. 3,5-Dimethyl-1H-pyrazol-4-ol is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and agrochemicals. It is synthesized through various chemical reactions, often involving the condensation of appropriate precursors. Due to its stability and reactivity, 3,5-dimethyl-1H-pyrazol-4-ol can be further functionalized or used as a building block in the synthesis of more complex molecules.

2820-38-4

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2820-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2820-38-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2820-38:
(6*2)+(5*8)+(4*2)+(3*0)+(2*3)+(1*8)=74
74 % 10 = 4
So 2820-38-4 is a valid CAS Registry Number.

2820-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Dimethyl-1H-pyrazol-4-ol

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-3,5-dimethyl-pyrazol

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:2820-38-4 SDS

2820-38-4Downstream Products

2820-38-4Relevant academic research and scientific papers

Nitrogen-containing heterocycles from metal β-diketonates

Svistunova,Shapkin,Nikolaeva,Apanasenko

experimental part, p. 756 - 761 (2011/08/06)

Factors determining the reaction of metal β-diketonates with hydrazine, in particular the nature of central metal ion and structure of β-diketonate ligand, are discussed. The possibility for the preparation of other heterocyclic compounds via reaction of metal acetylacetonates with phenylhydrazine, o-phenylenediamine, urea, and thiourea was studied.

Reactions of copper(II) β-diketonates under free radical conditions. Preparation of highly congested β-diketones

Lloris, Maria E.,Galvez, Nicanor,Marquet, Jorge,Moreno-Manas, Marcial

, p. 8031 - 8042 (2007/10/02)

Copper(II) β-diketonates react with alkyl bromides under free radical conditions to give highly congested β-diketones such as 3-(1-adamantyl)-3-alkylpentane-2,4-diones. Another typical free radical reagent: benzoyl peroxide, reacts also functionalizing the intercarbonyl positions.

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