499-49-0 Usage
Description
5-Methylisophthalic acid is an organic compound characterized by the presence of a methyl group attached to the isophthalic acid structure. It is a solid substance with potential applications in various industries due to its chemical properties.
Uses
Used in Chemical Synthesis:
5-Methylisophthalic acid is used as a chemical intermediate for the synthesis of a La(III)–Co(II) heterometallic framework. This application takes advantage of its ability to react with lanthanum(III) chloride hydrate and cobalt(II) acetate under ionothermal conditions, contributing to the formation of advanced materials with potential applications in various fields.
Used in Material Science:
In the field of material science, 5-Methylisophthalic acid can be utilized as a building block for the development of new materials with specific properties. Its solid-state nature and reactivity with metal salts make it a valuable component in the design and synthesis of novel materials with potential applications in areas such as catalysis, gas storage, and separation processes.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 5-Methylisophthalic acid may also find applications in the pharmaceutical industry. Its chemical structure could be exploited for the development of new drugs or drug delivery systems, taking advantage of its solid-state properties and reactivity with other compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 499-49-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 499-49:
(5*4)+(4*9)+(3*9)+(2*4)+(1*9)=100
100 % 10 = 0
So 499-49-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O4/c1-5-2-6(8(10)11)4-7(3-5)9(12)13/h2-4H,1H3,(H,10,11)(H,12,13)/p-2
499-49-0Relevant articles and documents
Hughes,Reid
, p. 516,521 (1949)
Surveying Iron-Organic Framework TAL-1-Derived Materials in Ligandless Heterogeneous Oxidative Catalytic Transformations of Alkylarenes
Alam, Mahboob,J?rving, Ivar,K??rik, Maike,Kongi, Nade?da,Leis, Jaan,Ping, Kefeng,Starkov, Pavel
supporting information, p. 1536 - 1540 (2019/08/07)
The use of carbonized materials derived from metal-organic frameworks (MOFs) in catalytic organic transformations is less well explored than is the use of MOFs. Here, we survey the oxidative performance of heterogeneous catalyst materials derived from the polycrystalline iron-organic framework TAL-1.
Aerobic oxidation of trimethylbenzenes catalyzed by N,N′,N″-trihydroxyisocyanuric acid (THICA) as a key catalyst
Hirai, Naruhisa,Tatsukawa, Yoshinobu,Kameda, Michiko,Sakaguchi, Satoshi,Ishii, Yasutaka
, p. 6695 - 6699 (2007/10/03)
The oxidation of trimethylbenzenes was examined with air or O2 using N,N′,N″-trihydroxyisocyanuric acid (THICA) as a key catalyst. Thus, 1,2,3-, 1,2,4-, and 1,3,5-trimethylbenzenes under air (20 atm) in the presence of THICA (5 mol %), Co(OAc)2 (0.5 mol %), Mn(OAc)2, and ZrO(OAc)2 at 150 °C were oxidized to the corresponding benzenetricarboxylic acids in good yields (81-97%). In the aerobic oxidation of 1,2,4-trimethylbenzene by the THICA/Co(II)/Mn(II) system, remarkable acceleration was observed by adding a very small amount of ZrO(OAc)2 to the reaction system to form 1,2,4-benzenetricarboxylic acid in excellent yield (97%). In contrast, no considerable addition effect was observed in the oxidation of 1,3,5-trimethylbenzene. This aerobic oxidation by the present catalytic system provides an economical and environmentally benign direct method to benzenetricarboxylic acids, which are very important polymer materials.
