Login   |   Create New Account sales@aaronchem.com

Home > Products> 735241-98-2
735241-98-2

4-(Chloromethyl)-1-methyl-1H-pyrazole hydrochloride

Catalog#: AR00FG1T  |   CAS#: 735241-98-2  |   MDL#: MFCD09859328  |   MF: C5H8Cl2N2  |   MW: 167.0364

Packsize Purity Price Availability Quantity
250mg 95% $500.00 3-4 weeks Buy Now Add To Cart
1g 95% $800.00 3-4 weeks Buy Now Add To Cart
  • Description
  • Application
  • Related Products
  • Featured Products
  • Safety Information
Catalog Number AR00FG1T
Chemical Name 4-(Chloromethyl)-1-methyl-1H-pyrazole hydrochloride
CAS Number 735241-98-2
Molecular Formula C5H8Cl2N2
Molecular Weight 167.0364
MDL Number MFCD09859328
SMILES ClCc1cnn(c1)C.Cl

4-(Chloromethyl)-1-methyl-1H-pyrazole is a versatile compound widely used in chemical synthesis due to its unique properties. 1. Alkylation Reactions: In chemical synthesis, 4-(Chloromethyl)-1-methyl-1H-pyrazole serves as an effective alkylating agent, allowing for the introduction of alkyl groups into various organic molecules. This facilitates the creation of new compounds with tailored properties and functionalities.2. Peptide Synthesis: The presence of the chloromethyl group in the compound enables it to participate in peptide synthesis reactions. By selectively reacting with amino acids or peptide fragments, 4-(Chloromethyl)-1-methyl-1H-pyrazole can be utilized in the assembly of complex peptide structures.3. Drug Development: The reactivity of 4-(Chloromethyl)-1-methyl-1H-pyrazole makes it a valuable tool in drug development processes. It can be employed in the modification of existing drugs or the synthesis of novel drug candidates by forming key chemical bonds within the molecular framework.4. Cross-Coupling Reactions: This compound can participate in cross-coupling reactions with various organic substrates, enabling the formation of C-C bonds and the synthesis of structurally intricate molecules. Such reactions are essential in the construction of diverse organic compounds.In summary, 4-(Chloromethyl)-1-methyl-1H-pyrazole plays a pivotal role in chemical synthesis by facilitating alkylation reactions, peptide synthesis, drug development, and cross-coupling reactions. Its unique reactivity and functional groups make it a valuable building block for creating a wide range of organic compounds with tailored properties and applications.
1194-96-3

1H-Pyrrole-2-carboxylic acid, 4-chloro-, methyl ester

1194-96-3

$35.00/100mg, $52.00/250mg, $104.00/1g, $312.00/5g, $520.00/10g, $1,039.00/25g, $1,645.00/50g,

59278-65-8

2-Amino-4-bromobenzaldehyde

59278-65-8

$4.00/100mg, $5.00/250mg, $6.00/1g, $18.00/5g, $34.00/10g, $76.00/25g, $285.00/100g,

1408168-69-3

Potassium (2-Methoxyethyl)trifluoroborate

1408168-69-3

$70.00/100mg, $122.00/250mg, $303.00/1g, $1,004.00/5g,

1408168-73-9

Potassium (2-(benzyloxy)ethyl)trifluoroborate

1408168-73-9

$11.00/100mg, $21.00/250mg, $47.00/1g, $139.00/5g, $231.00/10g, $572.00/25g, $970.00/50g, $1,558.00/100g,

744209-63-0

1H-Pyrrolo[2,3-b]pyridine, 4-chloro-1-(phenylsulfonyl)-

744209-63-0

$5.00/250mg, $13.00/1g, $30.00/5g, $54.00/10g, $122.00/25g, $208.00/50g, $381.00/100g,

160809-34-7

Benzyl 4-acetylpiperidine-1-carboxylate

160809-34-7

$52.00/250mg, $134.00/1g, $466.00/5g, $922.00/10g,

GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H332-H335
Precautionary Statements P280-P305+P351+P338-P310
Class N/A
Packing Group N/A

Home| Products| Terms & Conditions| Ordering & Shipping| Company| Contact us

© 2019 Aaron Chemicals LLC. All Rights Reserved.