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2498-50-2,MFCD00013001
Catalog No.:AA002PZZ

2498-50-2 | 4-Aminobenzamidine DiHCl

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$29.00   $20.00
- +
5g
98%
in stock  
$54.00   $38.00
- +
25g
98%
in stock  
$145.00   $102.00
- +
100g
98%
in stock  
$477.00 $334.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002PZZ
Chemical Name:
4-Aminobenzamidine DiHCl
CAS Number:
2498-50-2
Molecular Formula:
C7H11Cl2N3
Molecular Weight:
208.0883
MDL Number:
MFCD00013001
SMILES:
Nc1ccc(cc1)C(=N)N.Cl.Cl
Properties
Computed Properties
 
Complexity:
125  
Covalently-Bonded Unit Count:
3  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
5  
Rotatable Bond Count:
1  

Literature

Title: Discovery of benzothiazole guanidines as novel inhibitors of thrombin and trypsin IV.

Journal: Bioorganic & medicinal chemistry letters 20120715

Title: Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.

Journal: Nature chemical biology 20091001

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SDS
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Tags:2498-50-2 Molecular Formula|2498-50-2 MDL|2498-50-2 SMILES|2498-50-2 4-Aminobenzamidine DiHCl
Catalog No.: AA002PZZ
2498-50-2,MFCD00013001
2498-50-2 | 4-Aminobenzamidine DiHCl
Pack Size： 1g
Purity： 98%
in stock
$29.00 $20.00
Pack Size： 5g
Purity： 98%
in stock
$54.00 $38.00
Pack Size： 25g
Purity： 98%
in stock
$145.00 $102.00
Pack Size： 100g
Purity： 98%
in stock
$477.00 $334.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA002PZZ
Chemical Name: 4-Aminobenzamidine DiHCl
CAS Number: 2498-50-2
Molecular Formula: C7H11Cl2N3
Molecular Weight: 208.0883
MDL Number: MFCD00013001
SMILES: Nc1ccc(cc1)C(=N)N.Cl.Cl
Properties
Complexity: 125  
Covalently-Bonded Unit Count: 3  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 5  
Rotatable Bond Count: 1  
Literature fold

Title: Discovery of benzothiazole guanidines as novel inhibitors of thrombin and trypsin IV.

Journal: Bioorganic & medicinal chemistry letters20120715

Title: Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.

Journal: Nature chemical biology20091001

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