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Benzenemethanol, 2,4,5-trimethyl-3,6-dinitro-, also known as 2,4,5-trimethyl-3,6-dinitrobenzenemethanol, is an organic compound with the chemical formula C10H12N2O4. It is a derivative of benzenemethanol, featuring three methyl groups (CH3) at the 2, 4, and 5 positions, and two nitro groups (NO2) at the 3 and 6 positions on the benzene ring. Benzenemethanol, 2,4,5-trimethyl-3,6-dinitro- is characterized by its yellow crystalline appearance and has potential applications in the synthesis of pharmaceuticals and other organic compounds. Due to its complex structure and functional groups, it is essential to handle this chemical with care, as it may exhibit hazardous properties and require specific storage conditions.

88166-73-8

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88166-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88166-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,6 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88166-73:
(7*8)+(6*8)+(5*1)+(4*6)+(3*6)+(2*7)+(1*3)=168
168 % 10 = 8
So 88166-73-8 is a valid CAS Registry Number.

88166-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4,5-trimethyl-3,6-dinitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names 3,6-Dinitro-2,4,5-trimethylbenzylalcohol

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88166-73-8 SDS

88166-73-8Upstream product

88166-73-8Downstream Products

88166-73-8Relevant academic research and scientific papers

Oxidation of Aromatic Compounds. I. Oxidation of Methyl Derivatives of Nitrobenzene and Aniline in the System HSO3F-PbO2

Rudenko, A. P.,Korovina, N. S.,Aver'yanov, S. F.

, p. 1077 - 1083 (2007/10/03)

Low-temperature oxidation of methyl derivatives of nitrobenzene and aniline in the system HSO3F-PbO2 proceeds with intermediate formation of radical cations and results in replacement of hydrogen in one or two methyl groups or yields compounds of the diphenylmethane and biphenyl series.

THE ESR SPECTRA, STRUCTURE, AND REACTIVITY OF AROMATIC RADICAL-CATIONS IN SUPERACIDS

Rudenko, A. P.

, p. 1946 - 1980 (2007/10/03)

The oxidation of aromatic compounds by lead dioxide in superacids based on fluorosulfonic acid at -75 deg C takes place by a one-electron mechanism and leads in many cases to relatively stable radical-cations.The ESR spectra, the isotropic hyperfine coupling constants, data on the reactivity of the radical-cations, and the structures of the final products from their transformations under "long-life" conditions are presented.

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