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3-amino-2,4,6-triiodobenzoyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51935-27-4

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51935-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51935-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,3 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51935-27:
(7*5)+(6*1)+(5*9)+(4*3)+(3*5)+(2*2)+(1*7)=124
124 % 10 = 4
So 51935-27-4 is a valid CAS Registry Number.

51935-27-4Relevant academic research and scientific papers

Effect of contrast agent charge on visualization of articular cartilage using computed tomography: Exploiting electrostatic interactions for improved sensitivity

Joshi, Neel S.,Bansal, Prashant N.,Stewart, Rachel C.,Snyder, Brian D.,Grinstaff, Mark W.

supporting information; experimental part, p. 13234 - 13235 (2010/01/29)

(Chemical Equation Presented) The synthesis and evaluation of a new class of cationic iodinated contrast agents for the imaging of cartilage using computed tomography (CT) are described. In direct comparisons with anionic contrast agents, the cationic contrast agents afforded higher equilibrium concentrations in the articular cartilage of ex vivo rabbit femurs and thus greater imaging sensitivity. Variations in CT intensity across the sample reflected the inhomogeneous distribution of glycosaminoglycans in the tissue as confirmed by histological analysis. We anticipate that this work represents the first step in the development of sensitive, nondestructive CT-based methods to characterize the biochemical properties of cartilage using cationic contrast agents.

Chromatographic Separation of Enantiomers and Barriers to Enantiomerization of Axially Chiral Aromatic Carboxamides

Cuyegkeng, Maria Assunta,Mannschreck, Albrecht

, p. 803 - 810 (2007/10/02)

The enantiomers (M) and (P) of a series of similar aromatic carboxamides have been, for the first time, investigated analytically and enriched preparatively by liquid chromatography on triacetylcellulose.Enantiomeric purities (7-99percent), specific rotations, and barriers to rotation about the C(sp2)-C(sp2) bond (87 - 120 kJ/mol, Table 5) were determined.These energies are discussed in terms of the size of ortho substituents and of the buttressing effects by meta substituents.

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