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111573-59-2

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111573-59-2 Usage

General Description

3-(Dimethoxymethyl)-1H-pyrazole is a chemical compound with the molecular formula C7H12N2O2. It is a pyrazole derivative that contains two methoxy groups and a methoxymethyl group. This chemical has various applications in organic synthesis and pharmaceutical research due to its unique structure and properties. It can be used as a building block in the synthesis of various biologically active compounds and as a reagent in the formation of different heterocyclic compounds. Additionally, it has potential as a fungicide or pesticide due to its chemical properties. Overall, 3-(dimethoxymethyl)-1H-pyrazole is a versatile compound with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 111573-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,7 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111573-59:
(8*1)+(7*1)+(6*1)+(5*5)+(4*7)+(3*3)+(2*5)+(1*9)=102
102 % 10 = 2
So 111573-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O2/c1-9-6(10-2)5-3-4-7-8-5/h3-4,6H,1-2H3,(H,7,8)

111573-59-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H34057)  Pyrazole-3-carboxaldehyde dimethyl acetal, 95%   

  • 111573-59-2

  • 1g

  • 1462.0CNY

  • Detail
  • Alfa Aesar

  • (H34057)  Pyrazole-3-carboxaldehyde dimethyl acetal, 95%   

  • 111573-59-2

  • 5g

  • 4867.0CNY

  • Detail

111573-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Dimethoxymethyl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names BUTTPARK 858-12

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:111573-59-2 SDS

111573-59-2Relevant articles and documents

Synthetic method of tert-butyl-7-hydroxy-7,8-dihydro-4H-pyrazolo [1,5-a][1,4] diazepin-5-(6H)-carboxylate

-

Paragraph 0007, (2017/10/22)

The invention relates to a synthetic method of tert-butyl-7-hydroxy-7,8-dihydro-4H-pyrazolo [1,5-a][1,4] diazepin-5-(6H)-carboxylate and mainly solves the technical problems of low perfect ratio of a route, difficulty in reaction control, inconvenience in experiment operation and the like in the conventional synthetic process. Tert-butyl-7-hydroxy-7,8-dihydro-4H-pyrazolo [1,5-a][1,4] diazepin-5-(6H)-carboxylate is prepared from 1,1-dimethoxypropane-2-one serving as a starting material through six steps of reactions. The equation is shown in the specification. The obtained product diazepine is a useful intermediate or product for synthesis of various drugs.

Indium(III)trifluoromethanesulfonate as a mild, efficient catalyst for the formation of acetals and ketals in the presence of acid sensitive functional groups

Gregg, Brian T.,Golden, Kathryn C.,Quinn, John F.

, p. 3287 - 3295 (2008/09/21)

Aldehydes and ketones, including acetophenone and benzophenone, are readily protected under mild, neutral conditions in the presence of various alcohols or orthoformates and catalytic amounts of indium(III) trifluoromethanesulfonate (0.8 mol %) under either room temperature or mild heating conditions to give the corresponding cyclic and acyclic acetals and ketals in good to excellent yields. Acid sensitive functional groups, N-Boc, THP, and TBDMS do not undergo competitive deprotection under the reported conditions.

Synthesis and biological activities of meribendan and related heterocyclic benzimidazolo-pyridazinones

Jonas, R,Klockow, M,Lues, I,Pruecher, H,Schliep, H J,Wurziger, H

, p. 129 - 140 (2007/10/02)

The synthesis of a new heterocyclic benzimidazolo-pyridazinones is described.The new compounds were evaluated as inotropic agents with 'calcium-sensitizing' effects. 5-Methyl-6--2,3,4,5-tetrahydro-pyridazin-3-one hydrochloride (meribendan) turned out to be the most interesting compound and was chosen for development as a positive inotrope. benzimidazole / calcium sensivity / cardiotonics / inotropes / phosphodiesterase / papillary muscle / pyridazinone

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