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Benzenemethanol, 2,4,6-trimethyl-, nitrate is an organic compound with the chemical formula C10H15NO3. It is derived from benzenemethanol, a type of alcohol, by substituting three hydrogen atoms on the benzene ring with methyl groups (CH3) at the 2, 4, and 6 positions, and then adding a nitrate (NO3) group. Benzenemethanol, 2,4,6-trimethyl-, nitrate is characterized by its unique structure, which contributes to its specific chemical properties and potential applications. It is important to note that the nitrate group can be a source of concern due to its potential to form explosive compounds under certain conditions, and thus, handling and storage of such chemicals require careful consideration of safety protocols.

63548-90-3

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63548-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63548-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63548-90:
(7*6)+(6*3)+(5*5)+(4*4)+(3*8)+(2*9)+(1*0)=143
143 % 10 = 3
So 63548-90-3 is a valid CAS Registry Number.

63548-90-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-Trimethylbenzylnitrat

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:63548-90-3 SDS

63548-90-3Downstream Products

63548-90-3Relevant academic research and scientific papers

A NOVEL CLEAVAGE WITH NITRIC ACID OF POLYMETHYLATED DIBENZYL SELENIDES AND SELENOXIDES

Suzuki, Hitomi,Ohnishi, Kazumasa

, p. 111 - 112 (2007/10/02)

When treated with nitric acid at low temperature, the title selenides and selenoxides undergo a novel cleavage reaction to give the corresponding benzyl nitrates and elemental selenium.

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