71590-08-4 Usage
Description
METHYL 5-METHOXY-ISOPHTHALATE is a chemical compound derived from isophthalic acid, featuring a methyl and a methoxy group on the 5th and 3rd carbon atoms, respectively. It is primarily utilized in the production of ballpoint pen inks and dye intermediates, as well as in the synthesis of polyesters for various industrial applications.
Uses
Used in Ink Production:
METHYL 5-METHOXY-ISOPHTHALATE is used as a key component in the formulation of ballpoint pen inks, providing the necessary color and stability for writing.
Used in Dye Intermediates:
It serves as a dye intermediate, contributing to the production of various dyes used in different industries.
Used in Textile Industry:
METHYL 5-METHOXY-ISOPHTHALATE is used as a raw material for synthesizing polyesters, which are widely used in the textile industry for producing fabrics with desirable properties such as strength, durability, and wrinkle resistance.
Used in Packaging Industry:
In the packaging industry, METHYL 5-METHOXY-ISOPHTHALATE is used in the production of polyester films and containers, known for their lightweight, transparency, and resistance to moisture and chemicals.
Used in Automotive Industry:
It is employed in the synthesis of polyesters for automotive applications, such as in the production of lightweight and durable components, contributing to fuel efficiency and reduced emissions.
Used in Coating and Adhesive Products:
METHYL 5-METHOXY-ISOPHTHALATE is used as a component in the formulation of coating and adhesive products, providing properties like adhesion, flexibility, and resistance to environmental factors.
METHYL 5-METHOXY-ISOPHTHALATE is considered to be relatively low in toxicity and poses minimal environmental risk when handled and disposed of properly, making it a suitable choice for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 71590-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,9 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71590-08:
(7*7)+(6*1)+(5*5)+(4*9)+(3*0)+(2*0)+(1*8)=124
124 % 10 = 4
So 71590-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O5/c1-14-8-4-6(9(11)12)3-7(5-8)10(13)15-2/h3-5H,1-2H3,(H,11,12)
71590-08-4Relevant articles and documents
Cobalt(III)-Catalyzed Construction of Benzofurans, Benzofuranones and One-Pot Orthogonal C?H Functionalizations to Access Polysubstituted Benzofurans
Bera, Sourav Sekhar,Debbarma, Suvankar,Jana, Sripati,Maji, Modhu Sudan
supporting information, p. 2204 - 2210 (2018/06/07)
Benzofuran and benzofuranone derivatives have been synthesized through exclusive 5-exo-dig intramolecular hydroarylation using the amide-directed, cost-effective, high-valent Cp*CoIII-catalytic system. Challenging one-pot, orthogonal C?H functionalizations using two different electrophiles are also reported to afford polysubstituted benzofurans. Several valuable functional group interconversions along with removal of the amide directing group provide a route to access several diversely functionalized benzofurans. The mechanistic study suggests a reversible cobaltation step is operative here. (Figure presented.).
Hydroxylated 1,2,4-oxadiazole benzoic acid compounds, composistions thereof and the use for nonsense suppression
-
Page/Page column 10, (2008/12/06)
Novel hydroxylated 1,2,4-oxadiazole benzoic acid compounds, methods of using and pharmaceutical compositions comprising a hydroxylated 1,2,4-oxadiazole benzoic acid derivative are disclosed. The methods include methods of treating or preventing a disease
Inhibitors of the FEZ-1 metallo-β-lactamase
Lienard, Benoit M.R.,Horsfall, Louise E.,Galleni, Moreno,Frere, Jean-Marie,Schofield, Christopher J.
, p. 964 - 968 (2008/12/23)
Metallo-β-lactamases (MBLs) catalyze the hydrolysis of β-lactams including penicillins, cephalosporins and carbapenems. Starting from benzohydroxamic acid (1) structure-activity studies led to the identification of selective inhibitors of the FEZ-1 MBL, e.g., 2,5-substituted benzophenone hydroxamic acid 17 has a Ki of 6.1 ± 0.7 μM against the FEZ-1 MBL but does not significantly inhibit the IMP-1, BcII, CphA or L1 MBLs.
