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6,8-Dimercapto-octanoic acid benzylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76030-93-8

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76030-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76030-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,3 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76030-93:
(7*7)+(6*6)+(5*0)+(4*3)+(3*0)+(2*9)+(1*3)=118
118 % 10 = 8
So 76030-93-8 is a valid CAS Registry Number.

76030-93-8Relevant academic research and scientific papers

Neighboring Effect of Mercapto Group in the Silver Ion-promoted Aminolysis of S-Monoacyldihydrolipoamide

Nambu, Yoko,Endo, Takeshi,Okawara, Makoto

, p. 3433 - 3437 (1981)

The aminolysis of N-benzyl-8-S-(p-nitrobenzoyl)dihydrolipoamide has been enhanced remarkably with excess silver perchlorate compared with that of N-benzyl-S,S'-bis(p-nitrobenzoyl)dihydrolipoamide.From the results of kinetics and complex formation followed

Photoinduced enhancement in the luminescence of hydrophilic quantum dots coated with photocleavable ligands

Impellizzeri, Stefania,McCaughan, Bridgeen,Callan, John F.,Raymo, Francisco M.

, p. 2276 - 2283 (2012/03/10)

In search of strategies to photoactivate the luminescence of semiconductor quantum dots, we devised a synthetic approach to attach photocleavable 2-nitrobenzyl groups to CdSe-ZnS core-shell quantum dots coated with hydrophilic polymeric ligands. The emission intensity of the resulting nanostructured constructs increases by more than 60% with the photolysis of the 2-nitrobenzyl appendages. Indeed, the photoinduced separation of the organic chromophores from the inorganic nanoparticles suppresses an electron-transfer pathway from the latter to the former and is mostly responsible for the luminescence enhancement. However, the thiol groups anchoring the polymeric envelope to the ZnS shell also contribute to the photoinduced emission increase. Presumably, their photooxidation eliminates defects on the nanoparticle surface and promotes the radiative deactivation of the excited quantum dots. This effect is fully reversible but its magnitude is only a fraction of the change caused by the photocleavage of the 2-nitrobenzyl groups. In addition, these particular quantum dots can cross the membrane of model cells and their luminescence increases by ~80% after the intracellular photocleavage of the 2-nitrobenzyl quenchers. Thus, photoswitchable luminescent constructs with biocompatible character can be assembled combining the established photochemistry of the 2-nitrobenzyl photocage with the outstanding photophysical properties of semiconductor quantum dots and the hydrophilic character of appropriate polymeric ligands.

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