517-60-2 Usage
Description
MELLITIC ACID, also known as benzenehexacarboxylic acid, is a benzene-derived hexacarboxylic acid in which each carbon of benzene carries a carboxy substituent. It is characterized by its beige powder appearance and belongs to the group of benzenepolycarboxylic acids. MELLITIC ACID possesses potential anti-hemorrhagic properties and is also utilized as a motif for investigating possible radial self-assembly using complementary aromatic bases.
Uses
Used in Pharmaceutical Industry:
MELLITIC ACID is used as an active pharmaceutical ingredient for its potential anti-hemorrhagic properties, which can be beneficial in the development of treatments for various bleeding disorders and conditions.
Used in Chemical Research:
MELLITIC ACID serves as a motif in chemical research, specifically for investigating the radial self-assembly of complementary aromatic bases. This application contributes to the advancement of knowledge in the field of molecular self-assembly and its potential applications in material science and nanotechnology.
Used in Material Science:
As a part of benzenepolycarboxylic acids, MELLITIC ACID can be utilized in the development of new materials with specific properties, such as enhanced stability or reactivity, due to its unique chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 517-60-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 517-60:
(5*5)+(4*1)+(3*7)+(2*6)+(1*0)=62
62 % 10 = 2
So 517-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H6O12/c13-7(14)1-2(8(15)16)4(10(19)20)6(12(23)24)5(11(21)22)3(1)9(17)18/h(H,13,14)(H,15,16)(H,17,18)(H,19,20)(H,21,22)(H,23,24)
517-60-2Relevant articles and documents
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Wibaut et al.
, p. 742,744, 745 (1941)
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Schulz,Howard
, p. 991,993 (1946)
Access to aryl mellitic acid esters through a surprising oxidative esterification reaction
Geraskina, Margarita R.,Juetten, Mark J.,Winter, Arthur H.
, p. 5334 - 5337 (2014/06/23)
A serendipitously discovered oxidative esterification reaction of cyclohexane hexacarboxylic acid with phosphorus pentachloride and phenols provides one-pot access to previously unknown aryl mellitic acid esters. The reaction features a solvent-free digestion and chromatography-free purifications and demonstrates the possibility of cyclohexane-to-benzene conversions under relatively mild, metal-free conditions.
