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1,3-bis[(4-imidazolyl-methyl)aminomethyl]-5-[(4,6-dimethylpyridin-2-yl)aminomethyl]-2,4,6-triethylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1269804-77-4

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1269804-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1269804-77-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,8,0 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1269804-77:
(9*1)+(8*2)+(7*6)+(6*9)+(5*8)+(4*0)+(3*4)+(2*7)+(1*7)=194
194 % 10 = 4
So 1269804-77-4 is a valid CAS Registry Number.

1269804-77-4Upstream product

1269804-77-4Downstream Products

1269804-77-4Relevant academic research and scientific papers

Recognition properties of receptors consisting of imidazole and indole recognition units towards carbohydrates

Mazik, Monika,Hartmann, Andre

experimental part, (2010/07/18)

Compounds 4 and 5, including both 4(5)-substituted imidazole or 3-substituted indole units as the entities used in nature, and 2-aminopyridine group as a heterocyclic analogue of the asparagine/glutamine primary amide side chain, were prepared and their binding properties towards carbohydrates were studied. The design of these receptors was inspired by the binding motifs observed in the crystal structures of protein-carbohydrate complexes. 1H NMR spectroscopic titrations in competitive and non-competitive media as well as binding studies in two-phase systems, such as dissolution of solid carbohydrates in apolar media, revealed both highly effective recognition of neutral carbohydrates and interesting binding preferences of these acyclic compounds. Compared to the previously described acyclic receptors, compounds 4 and 5 showed significantly increased binding affinity towards β-galactoside. Both receptors display high β-vs. α-anomer binding preferences in the recognition of glycosides. It has been shown that both hydrogen bonding and interactions of the carbohydrate CH units with the aromatic rings of the receptors contribute to the stabilization of the receptor-carbohydrate complexes. The molecular modeling calculations, synthesis and binding properties of 4 and 5 towards selected carbohydrates are described and compared with those of the previously described receptors.

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