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Morpholine, 4-[[(4-nitrophenyl)imino]methyl]-, also known as 4-(4-Nitrophenylideneamino)morpholine, is an organic compound with the chemical formula C10H12N4O3. It is a derivative of morpholine, a heterocyclic organic compound with a six-membered ring containing two oxygen atoms and two nitrogen atoms. The compound features a 4-nitrophenyl group connected to the morpholine ring through an imine linkage, which is formed by the condensation of a primary amine with a nitro compound. This specific compound is characterized by its yellow crystalline appearance and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is important to note that due to the presence of the nitro group, Morpholine, 4-[[(4-nitrophenyl)imino]methyl]- may pose certain hazards and should be handled with care, following appropriate safety guidelines.

3616-86-2

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3616-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3616-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3616-86:
(6*3)+(5*6)+(4*1)+(3*6)+(2*8)+(1*6)=92
92 % 10 = 2
So 3616-86-2 is a valid CAS Registry Number.

3616-86-2SDS

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 1-morpholin-4-yl-N-(4-nitrophenyl)methanimine

1.2 Other means of identification

Product number -
Other names N2-p-nitrophenyl-N1,N1-cyclo(ethyleneoxyethylene)formamide

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:3616-86-2 SDS

3616-86-2Downstream Products

3616-86-2Relevant academic research and scientific papers

Amidines. Part 31. pKa Values of N1,N1-Dialkyl-N2-phenylformamidines in Water-Ethanol Solutions

Oszczapowicz, Janusz,Jaroszewska-Manaj, Jolanta

, p. 1677 - 1680 (2007/10/02)

The pKa values of three series (30 compounds in all) of N1,N1-dialkyl-N2-phenylformamidines (XC6H4N=CHNRR) have been measured in water-ethanol mixtures.The obtained pKa values of the amidines have been correlated with Hammett-type substituent constants and the pKa values of the corresponding primary amines determined in the same solvent.The applicability of various ? values is discussed and it is shown that, in each case, for substituents on the phenyl ring at the amino nitrogen atom ?0 values should be used.It is found that the slopes of regression lines for correlations with Hammett-type constants depend on the substituents at the amino nitrogen atom, as well as on the solvent.

Amidines. Part 20. Rate of Reaction of N,N-Dialkylformamide Acetals with Substituted Anilines

Osek, Jerzy,Oszczapowicz, Janusz,Drzewinski, Witold

, p. 1961 - 1964 (2007/10/02)

Rate of reaction of seven N,N-dialkylformamide acetals R2N-CH(OR2)2 with a series of anilines substituted on the phenyl ring have been measured in benzene, methanol, chloroform, and tetrahydrofuran by use of a g.l.c. method.In each case studied reaction is irreversible and obeys a second-order kinetic equation.Reaction rates correlate with Hammett ? constants for substituents on the phenyl ring of the aniline molecule.On the basis of the kinetic data, the mechanism of reaction is discussed.

Thermolysis and Photolysis of Some 5-Amino-4-methoxycarbonyl-Δ2-1,2,3-triazolines

Bourgois, J.,Mathieu, A.,Texier, F.

, p. 513 - 515 (2007/10/02)

Thermolysis of 5-amino-4-methyl-4-methoxycarbonyl-Δ2-1,2,3-triazolines leads to amidines and 1-methoxycarbonyl diazoethane.If the N1 substituent is a tosyl or benzoyl group, the corresponding triazoline is not isolated, the azide addition to the olefin gives directly the thermolysis products at room temperature.Triazoline photolysis leads to amino aziridines which are azomethine ylids.

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