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2-Nitro-4-[(E)-2-nitroethenyl]phenol is an organic compound characterized by its molecular formula C8H6N2O5. 2-nitro-4-[(E)-2-nitroethenyl]phenol features a phenol backbone with a nitro group at the 2nd position and a nitroethenyl group at the 4th position. The nitroethenyl group is in the E configuration, indicating that the two nitro groups are on the same side of the double bond. This chemical is known for its potential applications in the synthesis of dyes and pharmaceuticals, as well as its use as an intermediate in chemical reactions. Due to the presence of multiple nitro groups, it is also important to consider its stability and potential reactivity, especially in the context of safety and handling procedures.

2084-92-6

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2084-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2084-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2084-92:
(6*2)+(5*0)+(4*8)+(3*4)+(2*9)+(1*2)=76
76 % 10 = 6
So 2084-92-6 is a valid CAS Registry Number.

2084-92-6SDS

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-nitro-4-[(E)-2-nitroethenyl]phenol

1.2 Other means of identification

Product number -
Other names 2-nitro-4-(2-nitroethenyl)phenol

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:2084-92-6 SDS

2084-92-6Downstream Products

2084-92-6Relevant academic research and scientific papers

Cold microwave chemistry: synthesis using pre-cooled reagents

Bose, Ajay K.,Ganguly, Subhendu N.,Manhas, Maghar S.,He, William,Speck, Jeffrey

, p. 3213 - 3215 (2006)

A novel experimental procedure for chemical reactions has been devised that involves mixing and then freezing the reagents (organic solvent-free) to a sub-zero temperature such as -30 °C. This frozen mixture is exposed to microwave irradiation for a brief period of time. The use of pre-cooled reagents may give a single product not obtained by traditional microwave irradiation at room temperature. Interestingly, such a product may provide information about mechanisms by identifying the first step of a multiple step reaction.

Microwave assisted synthesis of an unusual dinitro phytochemical

Bose, Ajay K.,Ganguly, Subhendu N.,Manhas, Maghar S.,Srirajan, Vaidyanathan,Bhattacharjee, Ashoke,Rumthao, Sochanchingwung,Sharma, Anju H.

, p. 1179 - 1181 (2004)

A novel dinitro secondary metabolite, 2-nitro-4-(2′-nitroethenyl) phenol has been isolated from a marine source. This metabolite was synthesized first (in 1964 in Japan) and discovered later (in 1991 in India) as a natural product. We describe here a new synthesis via highly accelerated, microwave assisted, nitration reactions using mild reagents. ipso-Substitution of a carboxy group by a nitro group is discussed.

Microwave promoted rapid nitration of phenolic compounds with calcium nitrate

Bose, Ajay K.,Ganguly, Subhendu N.,Manhas, Maghar S.,Rao, Sheetal,Speck, Jeffrey,Pekelny, Uri,Pombo-Villars, Esteban

, p. 1885 - 1888 (2006)

Highly accelerated and safe nitration of phenolic compounds has been found to be feasible with a mixture of calcium nitrate and acetic acid as an efficient nitration agent under brief microwave irradiation. This method is compatible with the green chemistry approach because calcium salts-the inorganic byproducts-can be useful agrochemicals rather than waste chemicals. Commercially available 15N-labeled calcium nitrate is convenient for the preparation of 15N-labeled compounds for metabolic studies and mass spectrometry. This safe nitration method can be included in laboratory experiments for high school and college students.

Nitration of cinnamic acids using cerium (IV) ammonium nitrate immobilized on silica

Messere, Anna,Gentili, Alessandra,Garella, Isidoro,Temussi, Fabio,Di Blasio, Benedetto,Fiorentino, Antonio

, p. 3317 - 3324 (2007/10/03)

Treatment of cinnamic acids with cerium (IV) ammonium nitrate supported on silica (CAN/SiO2) was used to synthesize nitro derivative and ipso substitution products. The position of the substituents defines the type and the yields of the product

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