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92234-54-3

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92234-54-3 Usage

Description

1-(1-Adamantyl)pyrazole is a chemical compound with the molecular formula C14H20N2, belonging to the class of substituted pyrazole derivatives. It features an adamantane group, which imparts unique structural and property characteristics to the molecule. 1-(1-Adamantyl)pyrazole has garnered interest due to its potential pharmaceutical applications and utility as a building block in organic synthesis. It demonstrates a spectrum of biological activities, such as anticonvulsant and neuroprotective effects, and is being explored for its possible role in treating neurodegenerative diseases. Furthermore, 1-(1-Adamantyl)pyrazole's potential as a corrosion inhibitor adds to its versatility, making it a valuable compound with a broad range of potential applications across different industries.

Uses

Used in Pharmaceutical Industry:
1-(1-Adamantyl)pyrazole is used as a pharmaceutical compound for its anticonvulsant and neuroprotective effects, making it a candidate for the development of treatments for various neurological conditions and neurodegenerative diseases.
Used in Organic Synthesis:
1-(1-Adamantyl)pyrazole is used as a building block in organic synthesis, contributing to the creation of new and complex molecules with potential applications in various fields, including pharmaceuticals, materials science, and chemical research.
Used in Corrosion Inhibition:
1-(1-Adamantyl)pyrazole is used as a corrosion inhibitor, leveraging its unique properties to protect materials from degradation in various industrial applications, particularly in the manufacturing and maintenance of metal structures and equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 92234-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,3 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92234-54:
(7*9)+(6*2)+(5*2)+(4*3)+(3*4)+(2*5)+(1*4)=123
123 % 10 = 3
So 92234-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2/c1-2-14-15(3-1)13-7-10-4-11(8-13)6-12(5-10)9-13/h1-3,10-12H,4-9H2

92234-54-3SDS

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 1-(1-adamantyl)pyrazole

1.2 Other means of identification

Product number -
Other names adamantanylpyrazole

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:92234-54-3 SDS

92234-54-3Relevant articles and documents

Synthesis and reactivity of new 1-(1-adamantyl)pyrazoles

Cabildo,Claramunt,Elguero

, p. 249 - 251 (1984)

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Electrochemical Decarboxylative N-Alkylation of Heterocycles

Baran, Phil. S.,He, Chi,Shang, Ming,Sheng, Tao,Vantourout, Julien. C.,Zhang, Hai-Jun

supporting information, p. 7594 - 7598 (2020/10/09)

An operationally simple method to employ nonactivated carboxylic acids as alkylating agents in the N-alkylation of heterocycles is reported through an electrochemically driven anodic decarboxylative process. A wide substrate scope across a range of heterocycles is demonstrated along with a series of applications that significantly reduce the step count required to access such medicinally relevant structures.

Adamantylation of azoles with 1,3-dehydroadamantane. Selective N-adamantylation of pyrazoles

Butov,Mokhov,Parshin,Lysykh,Konyushkin,Firgang

experimental part, p. 150 - 151 (2011/04/24)

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