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1-(2-chloroethyl)-5-methyl-pyrazole is a chemical compound characterized by the molecular formula C6H8ClN3. It is a pyrazole derivative featuring a chloroethyl group at the first position and a methyl group at the fifth position of the pyrazole ring. 1-(2-chloroethyl)-5-methyl-pyrazole is recognized for its potential medicinal properties and is commonly utilized in the pharmaceutical industry.

96450-54-3

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96450-54-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-chloroethyl)-5-methyl-pyrazole is used as an enzyme inhibitor for its potential medicinal properties. Its unique structural features contribute to its value in the development of pharmaceuticals, particularly those targeting specific enzyme pathways.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-chloroethyl)-5-methyl-pyrazole serves as a building block for creating new compounds with biological activity. Its structural composition allows for the synthesis of a variety of molecules with potential applications in various industries.
Used in Medicinal Chemistry Research:
1-(2-chloroethyl)-5-methyl-pyrazole is also utilized as a valuable tool in medicinal chemistry research. Its structural attributes make it an important compound for studying and understanding the interactions between biological molecules and potential drug candidates.
Used in Chemical Research and Development:
1-(2-chloroethyl)-5-methyl-pyrazole's unique structure and properties make it a useful tool in the broader field of chemical research and development. It can be employed to explore new reactions, mechanisms, and the development of novel chemical entities with potential applications in various sectors, including but not limited to pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 96450-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,5 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96450-54:
(7*9)+(6*6)+(5*4)+(4*5)+(3*0)+(2*5)+(1*4)=153
153 % 10 = 3
So 96450-54-3 is a valid CAS Registry Number.

96450-54-3 Well-known Company Product Price

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  • Aldrich

  • (CBR00210)  1-(2-Chloroethyl)-5-methyl-1H-pyrazole  AldrichCPR

  • 96450-54-3

  • CBR00210-1G

  • 2,575.17CNY

  • Detail

96450-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloroethyl)-5-methylpyrazole

1.2 Other means of identification

Product number -
Other names BB_SC-5010

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:96450-54-3 SDS

96450-54-3Downstream Products

96450-54-3Relevant academic research and scientific papers

Aqueous N-methylmorpholine N-oxide as a new medium for alkylation of pyrazoles

Hasratyan, Ani H.,Alexanyan, Ashkharuhi G.,Khachatryan, Hasmik N.,Zakaryan, Geghetsik B.,Hayotsyan, Sargis S.,Danagulyan, Gevorg G.,Attaryan, Hovhannes S.

, p. 751 - 754 (2018/09/19)

[Figure not available: see fulltext.] It is shown that alkylation of pyrazoles with (E)/(Z)-1,3-dichlorobut-2-enes can be carried out in an alkaline aqueous medium in the presence of N-methylmorpholine N-oxide. In some cases, this technique may substitute

Synthesis of N-vinylpyrazoles

Attarian,Matsoyan,Martirosyan

, p. 452 - 455 (2007/10/03)

A method is proposed for the alkylation of pyrazoles with dichloroethane in water in the presence of the phase-transfer catalyst benzyltriethylammonium chloride (TEBAC). It was shown that dehydrochlorination of the corresponding N-(β-chloroethyl)pyrazoles in water under conditions of phase-transfer catalysis proceeds smoothly with the formation of N-vinylpyrazoles in 80-90% yield. 2005 Springer Science+Business Media, Inc.

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