124-42-5 | Acetamidine hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
25g	95%	in stock	$13.00	$9.00
100g	95%	in stock	$26.00	$18.00
500g	95%	in stock	$69.00	$49.00

Description

• Catalog Number: AA27491
• Chemical Name: Acetamidine hydrochloride
• CAS Number: 124-42-5
• Molecular Formula: C2H7ClN2
• Molecular Weight: 94.5434
• MDL Number: MFCD00013016
• SMILES: CC(=N)N.Cl
• NSC Number: 7595

Computed Properties

• Complexity: 31
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 3

Upstream Synthesis Route

Acetamidine Hydrochloride is a versatile chemical compound widely used in chemical synthesis for various applications. In organic chemistry, it is commonly employed as a reagent in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Acetamidine Hydrochloride serves as a key building block in the synthesis of various organic compounds, playing a crucial role in creating complex molecular structures. Its unique properties make it an essential component in the development of new drugs, such as antiviral and antibacterial agents. Moreover, Acetamidine Hydrochloride is a valuable tool in the field of medicinal chemistry, facilitating the creation of bioactive molecules with potential therapeutic applications. In summary, Acetamidine Hydrochloride is a fundamental reagent that enables chemists to carry out intricate chemical transformations and advance the field of chemical synthesis.

Literature

• Novel aminobenzyl-acetamidine derivative modulate the differential regulation of NOSs in LPS induced inflammatory response: role of PI3K/Akt pathway.

  Biochimica et biophysica acta 20121201

• Selective inhibition of inducible nitric oxide synthase by derivatives of acetamidine.

  Medicinal chemistry (Shariqah (United Arab Emirates)) 20121101

• A mild liquid reduction route toward uniform blue-emitting EuCl2 nanoprisms and nanorods.

  Inorganic chemistry 20110801

• Selective inhibition of iNOS by benzyl- and dibenzyl derivatives of N-(3-aminobenzyl)acetamidine.

  ChemMedChem 20110704

• A synthesis of acetamidines.

  The Journal of organic chemistry 20110318

• Characterization and inactivation of an agmatine deiminase from Helicobacter pylori.

  Bioorganic chemistry 20100401

• Haloacetamidine-based inactivators of protein arginine deiminase 4 (PAD4): evidence that general acid catalysis promotes efficient inactivation.

  Chembiochem : a European journal of chemical biology 20100125

• Four-component synthesis of fully substituted 1,2,4-triazoles.

  Angewandte Chemie (International ed. in English) 20100101

• Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives.

  Chemical communications (Cambridge, England) 20081221

• Differential effects of selective and non-selective inhibition of nitric oxide synthase on the expression and activity of cyclooxygenase-2 during gastric ulcer healing.

  European journal of pharmacology 20060501