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1,3,5-Triazin-2-amine, 4,6-dichloro-N-(triphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33347-45-4

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33347-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33347-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,4 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33347-45:
(7*3)+(6*3)+(5*3)+(4*4)+(3*7)+(2*4)+(1*5)=104
104 % 10 = 4
So 33347-45-4 is a valid CAS Registry Number.

33347-45-4Relevant academic research and scientific papers

Preparation of antibodies and development of an enzyme-linked immunosorbent assay for determination of dealkylated hydroxytriazines

Sanvicens, Nuria,Pichon, Valerie,Hennion, Marie-Claire,Marco, M.-Pilar

, p. 156 - 164 (2003)

The development of an indirect competitive enzyme-linked immunosorbent assay (ELISA) for dealkylated hydroxytriazines is reported here for the first time. The assay uses polyclonal antibodies raised against N-(4-amine-6-hydroxy-[1,3,5]triazin-2-yl)-4-aminobutanoic acid (hapten 2g) conjugated to keyhole limpet hemocyanin by the active ester method. The immunizing hapten was synthesized by first introducing the amino group to the triazine ring in a protected form in order to increase its solubility in organic media. Subsequent steps consisted of reacting this compound with an appropriate spacer arm, followed by removal of the protecting group in acidic media. The resulting assay uses a homologous competitor hapten coupled to conalbumin by the mixed anhydride method. Coating antigens prepared using a homologous covalent coupling procedure failed to produce competitive immunoassays. The assay tolerates media with high ionic strength (up to 70 mS cm-1) and basic pH values (7.5-9.5 units). Under the optimized conditions, this ELISA is specific for dealkylated hydroxytriazines, reaching suitable limits of detection.

Targeting the erythrocytic and liver stages of malaria parasites with s-triazine-based hybrids

Rodrigues, Catarina A. B.,Frade, Raquel F. M.,Albuquerque, Inês S.,Perry, Maria J.,Gut, Jiri,Machado, Marta,Rosenthal, Philip J.,Prudêncio, Miguel,Afonso, Carlos A. M.,Moreira, Rui

, p. 883 - 890 (2015/05/05)

A diversity-oriented library of s-triazine-based hybrids was screened for activity against the chloroquine-resistant Plasmodium falciparum W2 strain. The most striking result was sub-micromolar activity against cultured erythrocytic-stage parasites of hybrid molecules containing one or two 8-aminoquinoline moieties. These compounds were not clearly toxic to human cells. The most effective blood-schizontocidal s-triazine derivatives were then screened for activity against the liver stage of malaria parasites. The s-triazine hybrid containing two 8-aminoquinoline moieties and one chlorine atom emerged as the most potent against P. berghei liver-stage infection, active in the low nanomolar region, combined with good metabolic stability in rat liver microsomes. These results indicate that s-triazine-8-aminoquinoline-based hybrids are excellent starting points for lead optimization as dual-stage antimalarials.

Synthesis and relaxometric properties of gadolinium(III) complexes of new triazine-based polydentate ligands

Tei, Lorenzo,Benzi, Marina,Kielar, Filip,Botta, Mauro,Cavallotti, Camilla,Giovenzana, Giovanni Battista,Aime, Silvio

experimental part, p. 2414 - 2426 (2010/03/25)

Two new derivatives based on an s-triazine structural motif were synthesized by attaching two 2,2′-hydrazinylidenebis[acetic acid] moieties to the triazine ring to reach an overall heptadenticity for the complexation of lanthanide(III) cations. The remain

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