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54915-41-2

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54915-41-2 Usage

General Description

(2-Methyl-6-nitrophenyl)Methanol, also known as 2,6-dinitro-4-methoxybenzaldehyde, is an organic compound with the molecular formula C8H9NO4. It belongs to the class of nitrophenyl alcohols, which are commonly used as intermediates in the synthesis of pharmaceuticals, agrochemicals, and dyes. (2-Methyl-6-nitrophenyl)Methanol is a pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. It is primarily used as a reagent in organic synthesis, particularly in the preparation of various derivatives and analogs for research purposes. Additionally, it has been reported to possess antimicrobial and anticancer properties, making it a potentially valuable compound for further pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 54915-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,1 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54915-41:
(7*5)+(6*4)+(5*9)+(4*1)+(3*5)+(2*4)+(1*1)=132
132 % 10 = 2
So 54915-41-2 is a valid CAS Registry Number.

54915-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methyl-6-nitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-(hydroxymethyl)-3-methyl-1-nitrobenzene

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:54915-41-2 SDS

54915-41-2Relevant articles and documents

MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES RELATED THERETO

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Page/Page column 238; 241; 306-307, (2021/02/12)

This disclosure relates to compounds having pesticidal utility against pests in phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such compounds and intermediates used in such processes, compositions containing such compounds, and processes of using such compounds against such pests. These compounds/molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses compounds having the following formula (Formula One and/or Formula One-A).

INHIBITORS OF CYTOSOLIC PHOSPHOLIPASE A2

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Page/Page column 29-30, (2008/06/13)

This invention provides chemical inhibitors of the activity of various phospholipase enzymes, particularly cytosolic phospholipase A2 enzymes (cPLA2), more particularly including inhibitors of cytosolic phospholipase A2 alpha enzymes (cPLAα). In some embodiments, the inhibitors have the Formula I: wherein the constituent variables are as defined herein.

o-Nitroaryldioxolane for protection of pheromones. Study of the photodelivery of carbonylic compounds

Ceita, Luisa,Maiti, Amiya K.,Mestres, Ramon,Tortajada, Amparo

, p. 1023 - 1055 (2007/10/03)

o-Nitrophenyldioxolanes 1 to 12 have been prepared and the rate of their photocleavage determined Steric congestion in the molecule causes a decrease of the reaction rate. The decrease in the rate is especially important in the presence of a nitro group in a second phenyl ring.

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