857661
4-Aminobenzamidine dihydrochloride
98%
Synonym(s):
p-Aminobenzimidamide dihydrochloride
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About This Item
Linear Formula:
H2NC6H4C(=NH)NH2·2HCl
CAS Number:
Molecular Weight:
208.09
Beilstein:
3692927
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
crystals
mp
>300 °C (lit.)
functional group
amine
storage temp.
2-8°C
SMILES string
Cl[H].Cl[H].NC(=N)c1ccc(N)cc1
InChI
1S/C7H9N3.2ClH/c8-6-3-1-5(2-4-6)7(9)10;;/h1-4H,8H2,(H3,9,10);2*1H
InChI key
GHEHNICLPWTXJC-UHFFFAOYSA-N
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Application
4-Aminobenzamidine dihydrochloride can be used to synthesize:
- Orally active fibrinogen receptor antagonists based on benzamidines.[1]
- Benzamidine derivatives that are selective and potent serine protease inhibitors.[2][3]
- Novel pyrrolo [3,2-c] quinolines that are structural analogs of topoisomerase inhibitors such as coralyne and fagaronine.[4]
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Design of orally active, non-peptide fibrinogen receptor antagonists. An evolutionary process from the RGD sequence to novel anti-platelet aggregation agents.
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Bioorganic & Medicinal Chemistry, 2(9), 881-895 (1994)
In vitro blood compatibility of polymeric biomaterials through covalent immobilization of an amidine derivative.
Gouzy M F, et al.
Biomaterials, 25(17), 3493-3501 (2004)
A L Nguyen et al.
Biotechnology and bioengineering, 34(9), 1186-1190 (1989-11-01)
Reactive polymers have been prepared by copolymeriz-ing N-isopropyl acrylamide (NIPAM) with N-acryloxy-succinimide (NASI) or glycidyl methacrylate (GMA). The amino groups of ligands could react with the residues of NASI or GMA and the polymers could be precipitated by temperature and/or
A synthesis of new pyrrolo [3, 2?c] quinolines.
Dudouit F, et al.
Journal of Heterocyclic Chemistry, 38(3), 755-758 (2001)
A L Nguyen et al.
Enzyme and microbial technology, 12(9), 663-668 (1990-09-01)
A reactive water-soluble polymer was synthesized by copolymerizing N-isopropylacrylamide and glycidyl acrylate. The reactive polymer could react with the amino groups of enzymes/proteins or other ligands to form an affinity polymer. As a model, the reactive polymer was allowed to
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