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CAS

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15539-78-3

Benzenemethanol, 3-nitro-, nitrate (ester), also known as 3-Nitrobenzyl nitrate, is an organic compound with the chemical formula C7H6N2O4. It is a derivative of benzyl alcohol, where a nitro group is attached to the benzene ring at the 3rd position and a nitrate ester group is present at the benzylic position. Benzenemethanol, 3-nitro-, nitrate (ester) is characterized by its yellowish color and is sensitive to heat and shock, making it potentially explosive. It is used in the synthesis of various organic compounds and as an intermediate in the production of pharmaceuticals and other chemicals. Due to its reactivity, it is important to handle 3-Nitrobenzyl nitrate with caution and in accordance with proper safety protocols.

15539-78-3

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15539-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15539-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,3 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15539-78:
(7*1)+(6*5)+(5*5)+(4*3)+(3*9)+(2*7)+(1*8)=123
123 % 10 = 3
So 15539-78-3 is a valid CAS Registry Number.

15539-78-3Downstream Products

15539-78-3Relevant articles and documents

Oxidation of benzylic alcohols and ethers to carbonyl derivatives by nitric acid in dichloromethane

Strazzolini, Paolo,Runcio, Antonio

, p. 526 - 536 (2007/10/03)

Nitric acid in dichloromethane may be successfully employed for the oxidation of benzylic alcohols and ethers to the corresponding carbonyl compounds. The proposed method proved to be of general applicability, affording very good yields of aldehydes and ketones and showing interesting chemoselectivity in many instances, allowing competitive aromatic nitration to be avoided, as well as - in the case of aldehydes - any further oxidation to carboxylic acids. The reaction probably proceeds by a radical mechanism, the active species in the oxidation process being NO2. Competitive formation of nitro esters was observed in some cases, whereas poor results were obtained with allylic and non-benzylic substrates. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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