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Phenol, 2-methoxy-4-[2-nitro-1-(nitromethyl)ethyl]-, also known as 2-methoxy-4-[2-nitro-1-(nitromethyl)ethyl]phenol, is a complex organic compound with the molecular formula C9H10N2O5. It is a derivative of phenol, characterized by the presence of a methoxy group at the 2-position and a 2-nitro-1-(nitromethyl)ethyl group at the 4-position. Phenol, 2-methoxy-4-[2-nitro-1-(nitromethyl)ethyl]- is a yellow crystalline solid and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its complex structure and potential reactivity, it is important to handle Phenol, 2-methoxy-4-[2-nitro-1-(nitromethyl)ethyl]- with care, following proper safety protocols and guidelines.

6178-43-4

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6178-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6178-43-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,7 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6178-43:
(6*6)+(5*1)+(4*7)+(3*8)+(2*4)+(1*3)=104
104 % 10 = 4
So 6178-43-4 is a valid CAS Registry Number.

6178-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,3-dinitropropan-2-yl)-2-methoxyphenol

1.2 Other means of identification

Product number -
Other names Phenol,2-methoxy-4-[2-nitro-1-(nitromethyl)ethyl]

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:6178-43-4 SDS

6178-43-4Downstream Products

6178-43-4Relevant academic research and scientific papers

One-pot synthesis of 1 ,3-dinitroalkanes catalysed by nickel species

Gao, Min,Wei, Yu-Ping

, p. 146 - 148 (2013/07/05)

The reaction of aromatic aldehydes with nitromethane afforded a one-pot preparation of 1,3-dinitroalkanes in the presence of a nickel catalytic system. This efficient and simple method proceeded with moderate to high yields (56-99%) under mild conditions.

Heterogeneous catalysts in the preparation of 2-aryl-1,3-dinitropropanes from β-nitrostyrenes or benzaldehydes

Fierro,Rezende,Sepulveda-Boza,Reyes-Parada,Cassels

, p. 294 - 296 (2007/10/03)

The use of heterogeneous basic catalysts (KF, NaHCO3) in the preparation of 2-Aryl-1,3-dinitropropanes from β-nitrostyrenes or benzaldehydes is described, with one example followed kinetically by HPLC analysis of aliquots of the reaction.

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