60728-41-8 Usage
Description
1-Methyl 2-aminoterephthalate is an organic compound that features a methyl and an amino group attached to a terephthalate structure. This molecule is known for its potential applications in various chemical syntheses and its ability to form complexes with other molecules.
Uses
Used in Chemical Synthesis:
1-Methyl 2-aminoterephthalate is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable building block in organic chemistry.
Used in the Synthesis of Triarylphosphine Methyl:
1-Methyl 2-aminoterephthalate is used as a key component in the synthesis of triarylphosphine methyl compounds. These compounds are important in the development of new materials and catalysts for various industrial applications.
Used in the Synthesis of 4-(Hydroxymethyl)-2-iodobenzoate:
1-Methyl 2-aminoterephthalate serves as a starting material in the synthesis of 4-(hydroxymethyl)-2-iodobenzoate derivatives. These derivatives have potential applications in pharmaceuticals and agrochemicals due to their unique chemical properties.
Used in the Synthesis of 1-Methyl-2-diphenylphosphinoterepthalate:
1-Methyl 2-aminoterephthalate is utilized in the synthesis of 1-methyl-2-diphenylphosphinoterepthalate, which can be employed as a ligand in coordination chemistry. This ligand can form stable complexes with metal ions, finding use in catalysis and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 60728-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,2 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60728-41:
(7*6)+(6*0)+(5*7)+(4*2)+(3*8)+(2*4)+(1*1)=118
118 % 10 = 8
So 60728-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c1-14-9(13)6-3-2-5(8(11)12)4-7(6)10/h2-4H,10H2,1H3,(H,11,12)/p-1
60728-41-8Relevant articles and documents
Carboxyl Methyltransferase Catalysed Formation of Mono- and Dimethyl Esters under Aqueous Conditions: Application in Cascade Biocatalysis
Ashbrook, Chloe,Carnell, Andrew J.,Goulding, Ellie,Hatton, Harry,Johnson, James R.,Kershaw, Neil M.,McCue, Hannah V.,Rigden, Daniel J.,Ward, Lucy C.
supporting information, (2022/02/21)
Carboxyl methyltransferase (CMT) enzymes catalyse the biomethylation of carboxylic acids under aqueous conditions and have potential for use in synthetic enzyme cascades. Herein we report that the enzyme FtpM from Aspergillus fumigatus can methylate a broad range of aromatic mono- and dicarboxylic acids in good to excellent conversions. The enzyme shows high regioselectivity on its natural substrate fumaryl-l-tyrosine, trans, trans-muconic acid and a number of the dicarboxylic acids tested. Dicarboxylic acids are generally better substrates than monocarboxylic acids, although some substituents are able to compensate for the absence of a second acid group. For dicarboxylic acids, the second methylation shows strong pH dependency with an optimum at pH 5.5–6. Potential for application in industrial biotechnology was demonstrated in a cascade for the production of a bioplastics precursor (FDME) from bioderived 5-hydroxymethylfurfural (HMF).
