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1-Bromo-1-deoxy-tri-O-benzoylthreitol is a complex organic compound with the molecular formula C31H27BrO8. It is a derivative of threitol, a sugar alcohol, where one hydroxyl group has been replaced with a bromine atom, and three hydroxyl groups have been protected with benzoyl groups. 1-bromo-1-deoxy-tri-O-benzoylthreitol is often used in organic synthesis and carbohydrate chemistry as an intermediate or a protecting group for the synthesis of more complex molecules. The benzoyl groups can be removed under certain conditions, allowing for further functionalization of the molecule. Its chemical structure and properties make it a valuable tool in the field of organic chemistry, particularly in the synthesis of complex carbohydrates and other biologically active compounds.

7718-68-5

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7718-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7718-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7718-68:
(6*7)+(5*7)+(4*1)+(3*8)+(2*6)+(1*8)=125
125 % 10 = 5
So 7718-68-5 is a valid CAS Registry Number.

7718-68-5Downstream Products

7718-68-5Relevant academic research and scientific papers

Synthesis of Nitriles from Haloesters, Haloketones and Haloethers

Talekar, D. G.,Joshi, P. L.,Ramaiah, P.,Rao, A. S.

, p. 145 - 151 (2007/10/02)

The action of NaCN on haloesters, haloketones and haloethers has been studied.Haloesters wherein halogen and ester functions are located on adjacent carbon atoms, do not furnish the corresponding nitriles, whereas those with halogen and ester functions not located on adjacent carbon atoms, furnish the corresponding nitriles in good yields.The presence of hydroxy or ether function on the carbon adjacent to primary halide bearing carbon atom does not interfere in the reaction with cyanide. δ-Haloketones are transformed to ketonitriles, γ-Haloketones are transformed to cyclopropyl ketones and epoxyhalides to epoxynitriles.

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