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124-42-5,MFCD00013016
Catalog No.:AA000LAF

124-42-5 | Acetamidine hydrochloride

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
92%
in stock  
$12.00   $8.00
- +
100g
92%
in stock  
$22.00   $15.00
- +
500g
92%
in stock  
$26.00   $18.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA000LAF
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
Properties
Properties
 
BP:
129.78°C (rough estimate)  
Form:
Solid  
MP:
165-170 °C  
Refractive Index:
1.5500 (estimate)  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

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

Literature

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

Journal: Biochimica et biophysica acta 20121201

Title: Selective inhibition of inducible nitric oxide synthase by derivatives of acetamidine.

Journal: Medicinal chemistry (Shariqah (United Arab Emirates)) 20121101

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

Journal: Inorganic chemistry 20110801

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

Journal: ChemMedChem 20110704

Title: A synthesis of acetamidines.

Journal: The Journal of organic chemistry 20110318

Title: Characterization and inactivation of an agmatine deiminase from Helicobacter pylori.

Journal: Bioorganic chemistry 20100401

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

Journal: Chembiochem : a European journal of chemical biology 20100125

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

Journal: Angewandte Chemie (International ed. in English) 20100101

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

Journal: Chemical communications (Cambridge, England) 20081221

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

Journal: European journal of pharmacology 20060501

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