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5-N-[4-amino-6-(R)-1-phenylethylamino-1,3,5-triazin-2-yl]amino-17-N-[4-amino-6-(3-amino-2,2-dimethylpropylamino)-1,3,5-triazin-2-yl]amino-25,26,27,28-tetrapropoxycalix[4]arene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

444997-22-2

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444997-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444997-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,9,9 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 444997-22:
(8*4)+(7*4)+(6*4)+(5*9)+(4*9)+(3*7)+(2*2)+(1*2)=192
192 % 10 = 2
So 444997-22-2 is a valid CAS Registry Number.

444997-22-2Downstream Products

444997-22-2Relevant academic research and scientific papers

Kinetic stabilities of double, tetra-, and hexarosette hydrogen-bonded assemblies

Prins, Leonard J.,Neuteboom, Edda E.,Paraschiv, Vasile,Crego-Calama, Mercedes,Timmerman, Peter,Reinhoudt, David N.

, p. 4808 - 4820 (2002)

A study of the kinetic stabilities of hydrogen-bonded double, tetra-, and hexarosette assemblies, comprising 36, 72, and 108 hydrogen bonds, respectively, is described. The kinetic stabilities are measured using both chiral amplification and racemization experiments. The chiral amplification studies show that solvent polarity and temperature strongly affect the kinetic stabilities of these hydrogen-bonded assemblies. For example, the activation energy for the dissociation of a tetramelamine from a tetrarosette assembly, a process that involves the breakage of 24 hydrogen bonds, was determined at 98.7 ± 16.6 kJ mol-1 in chloroform and 172.8 ± 11.3 kJ mol-1 in benzene. Moreover, racemization studies with enantiomerically enriched assemblies reveal a strong dependence of the kinetic stability on the number and strength of the hydrogen bonds involved in assembly formation. The half-lives for double, tetra-, and hexarosette assemblies were found to be 8.4 min, 5.5 h, and 150 h in chloroform at 50 °C, respectively. For higher generations of these types of assemblies, the kinetic stabilities become so high that they can no longer measured in a direct manner.

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