857661
4-Aminobenzamidine dihydrochloride
98%
Sinonimo/i:
p-Aminobenzimidamide dihydrochloride
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1 G
CHF 40.80
10 G
CHF 185.00
50 G
CHF 834.00
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Cambia visualizzazione
1 G
CHF 40.80
10 G
CHF 185.00
50 G
CHF 834.00
About This Item
Formula condensata:
H2NC6H4C(=NH)NH2·2HCl
Numero CAS:
Peso molecolare:
208.09
Beilstein:
3692927
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
98%
Stato
crystals
Punto di fusione
>300 °C (lit.)
Gruppo funzionale
amine
Temperatura di conservazione
2-8°C
Stringa SMILE
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
GHEHNICLPWTXJC-UHFFFAOYSA-N
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Categorie correlate
Applicazioni
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]
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
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)
Specific adsorption of serine proteases on coated silica beads substituted with amidine derivatives.
S Khamlichi et al.
Journal of chromatography, 510, 123-132 (1990-06-27)
Amidine derivatives interact with serine proteases, the inhibition being due to interactions between amidine functions and the active sites of the enzymes. Five different types of amidine (substituted or unsubstituted) were coupled to coated silica beads, which had previously been
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
Design of orally active, non-peptide fibrinogen receptor antagonists. An evolutionary process from the RGD sequence to novel anti-platelet aggregation agents.
Bovy P R, et al.
Bioorganic & Medicinal Chemistry, 2(9), 881-895 (1994)
Biochemical and molecular modeling analysis of the ability of two p-aminobenzamidine-based sorbents to selectively purify serine proteases (fibrinogenases) from snake venoms.
De-Simone S G, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 822(1-2), 1-9 (2005)
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