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1,3-Cyclohexanedicarboxamide, 4-hydroxy-N,N',4-trimethyl-2-(2-methylphenyl)-6-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132599-13-4

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132599-13-4 Usage

Molecular structure

The compound has a cyclohexane ring with two carboxamide groups attached to positions 1 and 3, a hydroxy group at position 4, and a trimethyl-substituted amide group also at position 4.

Functional groups

The molecule contains several functional groups, including amide, hydroxy, and methyl groups, which can potentially interact with biological systems.

Structural complexity

The presence of a cyclohexane ring, multiple amide groups, and a methylphenyl group adds complexity to the molecule, making it a potentially interesting compound for various applications.

Industrial applications

Due to its structural complexity and functional groups, this chemical may have a range of industrial applications, such as in the synthesis of other complex organic compounds or as an intermediate in chemical reactions.

Pharmaceutical potential

The presence of functional groups that could interact with biological systems suggests that 1,3-Cyclohexanedicarboxamide, 4-hydroxy-N,N',4-trimethyl-2-(2-methylphenyl)-6-oxo- may have potential pharmaceutical applications, such as in the development of new drugs or as a building block for drug candidates.

Stability

The stability of the compound under various conditions (e.g., temperature, pH, etc.) is not provided in the material, but it would depend on the specific functional groups and their interactions with the surrounding environment.

Reactivity

The reactivity of 1,3-Cyclohexanedicarboxamide, 4-hydroxy-N,N',4-trimethyl-2-(2-methylphenyl)-6-oxo- would be influenced by the presence of its various functional groups, which could potentially participate in chemical reactions with other molecules.

Synthesis

The synthesis of this complex organic compound would likely involve multiple steps, including the formation of the cyclohexane ring, the introduction of the carboxamide groups, and the attachment of the hydroxy and trimethyl-substituted amide groups.

Purity

The purity of the compound would depend on the specific synthetic route used and the efficiency of the purification methods employed during its preparation.

Check Digit Verification of cas no

The CAS Registry Mumber 132599-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,9 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132599-13:
(8*1)+(7*3)+(6*2)+(5*5)+(4*9)+(3*9)+(2*1)+(1*3)=134
134 % 10 = 4
So 132599-13-4 is a valid CAS Registry Number.

132599-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-2-(2-methylphenyl)-N,N',4-trimethyl-6-oxocyclohexane-1,3-dicarboxamide

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-4-methyl-6-oxo-2-o-tolyl-cyclohexane-1,3-dicarboxylic acid bis-methylamide

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:132599-13-4 SDS

132599-13-4Relevant academic research and scientific papers

10H-Phenothiazines: A new class of enzyme inhibitors for inflammatory diseases

Sadanandam,Shetty, Meera M.,Rao, A. Bhaskar,Rambabu

body text, p. 197 - 202 (2009/04/07)

The phenothiazine nucleus is known for their inhibitory activity towards the regulatory enzymes that are contributing to diseases such as asthma, autoimmune diseases including allergic rheumatoid and encephalomyelitis. In this study a number of substitute

An Unusual Ring-Cleavage of 2,4-Di-N-methylcarbamoylcyclohexanones into Glutaconimide and Cinnamamides

Sadanandam, Yennu S.,Leelavathi, Panaganti,Ansari, Imtiaz A.

, p. 1147 - 1158 (2007/10/02)

3-Aryl-5-hydroxy-5-methyl-2,4-di-N-methylcarbamoylcyclohexanones (1a-h) under acidic and basic conditions underwent ring-cleavage to give 1,4-dimethylglutaconimide (3) and substituted N-methylcinnamamides (4a-h).The probable mechanism for the formation of

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