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N-methylidene-4-nitroaniline, also known as 4-nitro-N-methylbenzenamine, is an organic compound with the chemical formula C7H8N2O2. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. N-methylidene-4-nitroaniline is primarily used as an intermediate in the synthesis of various dyes, pharmaceuticals, and agrochemicals. Due to its reactivity and potential health hazards, it is important to handle N-methylidene-4-nitroaniline with care, following proper safety protocols.

6973-12-2

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6973-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6973-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6973-12:
(6*6)+(5*9)+(4*7)+(3*3)+(2*1)+(1*2)=122
122 % 10 = 2
So 6973-12-2 is a valid CAS Registry Number.

6973-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-nitrophenyl)methanimine

1.2 Other means of identification

Product number -
Other names 1-Nitro-4-isocyan-benzol

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:6973-12-2 SDS

6973-12-2Downstream Products

6973-12-2Relevant academic research and scientific papers

Stereospecific copper-catalyzed domino ring opening and sp3 C-H functionalization of activated aziridines with N-alkylanilines

Sengoden, Mani,Bhowmick, Abhisikta,Punniyamurthy, Tharmalingam

supporting information, p. 158 - 161 (2017/11/27)

Copper efficiently catalyzed nucleophilic ring opening, sp3 C-H functionalization, and C-N bond formation in the presence of tert-butyl hydroperoxide to afford functionalized imidazolidines starting from N-sulfonylaziridines and Nalkylanilines. The products were obtained in high optical purities (95 → 99% ee) with excellent functional group tolerance.

Substituted Bicyclic and Tricyclic Oxazolo-1,2,3-Triazole Systems: Ring Expansions to 1,3,4,5-Oxatriazines and Ring Contractions to 1,2,3-Triazaspiroalkane Derivatives

Butler, Richard N.,O'Shea, Donal F.

, p. 2797 - 2800 (2007/10/02)

Synthesis of a range of new bicyclic and tricyclic fused oxazolo-1,2,3-triazole systems is described.Treatment of these with acid caused transformations to substituted 1,3,4,5-oxatriazine and new 1,2,3-triazaspiroalkane systems which were isolated in high yields.Kinetic studies of the ring transformations indicated the presence of a delocalised carbocation intermediate and the mechanism of the ring expansion and contraction is discussed.

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