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5-Nitro-5-methyl-2-isopropyl-m-dioxan is an organic compound characterized by its molecular formula C7H13NO4. It features a dioxane ring structure with a methyl group (CH3) at the 5-position, an isopropyl group (C3H7) at the 2-position, and a nitro group (NO2) also at the 5-position. 5-Nitro-5-methyl-2-isopropyl-m-dioxan is known for its potential applications in the synthesis of pharmaceuticals and other chemical products due to its unique structural properties. It is important to handle 5-Nitro-5-methyl-2-isopropyl-m-dioxan with care, as the nitro group can make it sensitive to heat and shock, posing potential hazards.

5689-68-9

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5689-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5689-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5689-68:
(6*5)+(5*6)+(4*8)+(3*9)+(2*6)+(1*8)=139
139 % 10 = 9
So 5689-68-9 is a valid CAS Registry Number.

5689-68-9Downstream Products

5689-68-9Relevant academic research and scientific papers

Reduction of 5-alkyl-5-nitro-1,3-diheterocycloalkanes by sodium alcoholates

Zorin, V. V.,Kukovitskii, D. M.,Todres, Z. V.,Zlot-skii, S. S.,Rakhmankulov, D. L.

, p. 1635 - 1638 (2007/10/02)

In the reaction of 5-alkyl-5-nitro-1,3-diheterocycloalkanes containing oxygen and nitrogen as heteroatoms with sodium alcoholates in the corresponding alcohol 5-alkyl-1,3-diheterocycloalkanes, the corresponding aldehydes (or ketones), and diols are formed.A mechanism is proposed for the formation of the reaction products, including the stage of one-electron transfer from the alcoholate to the nitro group of the 5-alkyl-5-nitro-1,3-diheterocycloalkane.

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