101046-55-3 Usage
Molecular structure
A complex organic compound with a benzene ring connected to a hexanedioic acid chain, featuring various functional groups such as hydroxy, methyl, and methoxy groups.
Functional groups
Contains a hydroxy group (-OH), a methyl group (-CH3), and a methoxy group (-OCH3), which are all interconnected to form the unique structure of the compound.
Double bond
The compound has a Z-configuration double bond (C=C) within its structure, which affects its chemical properties and reactivity.
Carboxylic acid group
The hexanedioic acid portion of the compound contains two carboxylic acid groups (-COOH), which can participate in various chemical reactions and interactions.
Potential applications
This chemical may have potential applications in pharmaceuticals, as its structure suggests possible interactions with biological systems, such as binding to receptors or enzymes.
Further research needed
To determine the specific properties and potential uses of 2-[1-(2-Hydroxy-5-methyl-phenyl)-meth-(Z)-ylidene]-5-(2-methoxy-5-methyl-benzyl)-hexanedioic acid, further research and testing would be required, including studies on its solubility, stability, and bioavailability.
Check Digit Verification of cas no
The CAS Registry Mumber 101046-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,4 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101046-55:
(8*1)+(7*0)+(6*1)+(5*0)+(4*4)+(3*6)+(2*5)+(1*5)=63
63 % 10 = 3
So 101046-55-3 is a valid CAS Registry Number.
101046-55-3Relevant academic research and scientific papers
STUDIES IN CLAISEN REARRANGEMENT; NOVEL THERMAL TRANSFORMATION OF α-ARYLOXYMETHYLACRYLIC ACIDS AND THEIR DERIVATIVES
Gopalan, B.,Rajagopalan, K.,Sunitha, K.,Balasubramanian, K. K.
, p. 3153 - 3160 (2007/10/02)
α-Aryloxymethylacrylic acids and their derivatives have been found to undergo some novel thermal transformations leading to the formation of 'ene' dimers.The structure of the dimer has been revised on the basis of degradation studies, extensive spectral data and isolation of intermediates.
