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(6Z)-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidene-2-methoxycyclohexa-2,4-dien-1-one is a synthetic organic compound characterized by its complex structure, featuring a cyclohexa-2,4-dien-1-one ring with a methoxy group and an amino group attached. (6Z)-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidene-2-methoxycyclohexa-2,4-dien-1-one also incorporates a hydroxyl group and a 1,1-dimethylethyl group, which contribute to its unique properties and potential applications in the chemical and pharmaceutical industries.

25458-13-3

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25458-13-3 Usage

Uses

Used in Pharmaceutical Applications:
(6Z)-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidene-2-methoxycyclohexa-2,4-dien-1-one is used as an active pharmaceutical ingredient for its potential therapeutic effects. (6Z)-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidene-2-methoxycyclohexa-2,4-dien-1-one's unique structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Synthesis:
In the chemical industry, (6Z)-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidene-2-methoxycyclohexa-2,4-dien-1-one is used as a key intermediate in the synthesis of various complex organic molecules. Its versatile structure enables it to be a valuable building block for creating a wide range of compounds with diverse applications.
Used in Material Science:
(6Z)-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidene-2-methoxycyclohexa-2,4-dien-1-one is also utilized in material science for the development of novel materials with specific properties. (6Z)-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidene-2-methoxycyclohexa-2,4-dien-1-one's unique structure can be exploited to create materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity.
Used in Research and Development:
This synthetic organic compound is used as a research tool in academic and industrial laboratories. It can be employed to study various aspects of chemical and biological systems, such as understanding the interactions between molecules, investigating the mechanisms of chemical reactions, or developing new analytical techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 25458-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,5 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25458-13:
(7*2)+(6*5)+(5*4)+(4*5)+(3*8)+(2*1)+(1*3)=113
113 % 10 = 3
So 25458-13-3 is a valid CAS Registry Number.

25458-13-3SDS

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 (6Z)-6-[[(1-hydroxy-2-methylpropan-2-yl)amino]methylidene]-2-methoxycyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names -

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:25458-13-3 SDS

25458-13-3Downstream Products

25458-13-3Relevant academic research and scientific papers

Synthesis, Crystal Structures, and Magnetic Properties of New Hexanuclear MnIII2LnIII4 Complexes: SMM Behavior of the Terbium(III) Analogue

Roy, Shuvayan,Ghosh, Sagar,Martins, Daniel O. T. A.,Tuna, Floriana,Mohanta, Sasankasekhar

, p. 5191 - 5202 (2018)

This investigation reports the syntheses, crystal structures, and magnetic properties of a series of isomorphous hexanuclear MnIII2LnIII4 compounds of composition [MnIII2LnIII4L12L22(μ3-OH)4(μ1,3-Pivalate)6(NO3)2]·2CH3CN {Ln = Tb (1), Dy (2), Ho (3), Er (4)}, where H2L1 is the Schiff base ligand that is obtained by [1+1] condensation of 3-methoxysalicylaldehyde (HL2) with 2-amino-2-methyl-1-propanol. While the O(phenoxo)N(imine)O(alkoxo) pocket of the ligand [L1]2– binds a MnIII ion, the other pocket, O(methoxy)O(phenoxo), remains noncoordinated. In contrast, each of the O(methoxy)O(phenoxo) and O(phenoxo)O(aldehyde) sites of [L2]– is occupied by a LnIII ion. Additionally, there are four μ3-hydroxo, six μ1,3-pivalate, and two chelating nitrate ligands, stabilizing the hexanuclear cores. Magnetic susceptibility (2–300 K) and magnetization (M) data reveal significant anisotropy in 1–4. Detailed ac susceptibility measurements have revealed single molecule magnet (SMM) behavior in the TbIII analogue with Ueff = 11.12 cm–1 and τ0 = 1.04 × 10–7 s under a 1000 Oe dc field and Ueff = 10.42 cm–1 and τ0 = 1.62 × 10–7 s under a 3500 Oe dc field, while the other three analogues do not show slow relaxation of magnetization.

Synthesis, Crystal Structures, Magnetic Properties, and Fluorescence of Two Heptanuclear CoIII4LnIII3 Compounds (Ln = GdIII, DyIII): Multiple Relaxation Dynamics in the DyIII Analogue

Roy, Shuvayan,Hari, Nairita,Mohanta, Sasankasekhar

, p. 3411 - 3423 (2019)

This report describes the synthesis, crystal structures, magnetic and spectroscopic properties of two heptanuclear CoIII4LnIII3 systems of composition [CoIII4GdIII3L4(μ4-O)2(μ-OMe)2(μ1,3-OAc)4(H2O)2(NO3)2]·NO3·2CH3OH·2H2O (1) and [CoIII4DyIII3L4(μ4-O)2(μ-OMe)2(μ1,3-OAc)4(H2O)2(NO3)2]·NO3·3CH3OH·1.5H2O (2), where H2L is [1+1] condensation product of 3-methoxysalicylaldehyde and 2-amino-2-methyl-1-propanol. The heptametallic cores in 1 and 2 may be taken as consisted of two symmetry related trinuclear CoIIILnIIICoIII moieties and a central lanthanide center in such a way that each of the three metal ions of each of the two trinuclear moieties are bridged with the central lanthanide through bridging oxo/alkoxo/acetate ligands. DC magnetic measurements of 1 and 2 reveal very weak GdIII···GdIII antiferromagnetic interaction (J = –0.01 cm–1) in 1 and significant anisotropy in 2. Variable-temperature and variable-frequency ac susceptibility measurements of 2 reveal that it is a zero-field SMM with multiple relaxation dynamics. Above 5 K, two well resolved relaxation channels are observed; Ueff and τ0 are 51.4 cm–1 and 9.40 × 10–7 s for the slow relaxation channel and 24.3 cm–1 and 6.91 × 10–7 s for the fast relaxation channel. The characteristic DyIII based transitions, 4F9/2→6H15/2, 4F9/2→6H13/2 and 4F9/2→6H11/2, can be well assigned in the fluorescence spectrum of 2 at solid state. All in all, compound 2 is a bifunctional molecular material.

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