7595-91-7 Usage
Uses
Used in Organic Synthesis:
2,4:3,5-Di-O-methylene-D-idaric Acid is utilized as a key intermediate in organic synthesis for the production of various complex organic molecules. Its unique structure allows it to participate in a variety of chemical reactions, such as condensation, esterification, and rearrangement, which are crucial for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4:3,5-Di-O-methylene-D-idaric Acid is used as a building block for the development of new drugs. Its ability to form stable intermediates and participate in multiple types of chemical reactions makes it an ideal candidate for the synthesis of novel drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
2,4:3,5-Di-O-methylene-D-idaric Acid also finds application in the agrochemical industry, where it is used in the synthesis of new pesticides and other crop protection agents. Its versatility in organic synthesis allows for the creation of innovative compounds that can effectively control pests and diseases in agriculture.
Used in Specialty Chemicals:
In the specialty chemicals sector, 2,4:3,5-Di-O-methylene-D-idaric Acid is employed for the synthesis of unique compounds with specific properties. These compounds can be used in various applications, such as in the production of dyes, fragrances, and other high-value specialty chemicals.
Overall, 2,4:3,5-Di-O-methylene-D-idaric Acid is a versatile and valuable compound in the field of organic synthesis, with applications spanning across multiple industries, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential component in the development of new and innovative chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 7595-91-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7595-91:
(6*7)+(5*5)+(4*9)+(3*5)+(2*9)+(1*1)=137
137 % 10 = 7
So 7595-91-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O8/c1-13-9(11)7-5-6(16-3-17-7)8(10(12)14-2)18-4-15-5/h5-8H,3-4H2,1-2H3
7595-91-7Relevant academic research and scientific papers
Polyamides and polyesters containing 2,4:3,5-di-O-methylene-L-idaroyl residues
Tinnemans, A. H. A.,Budding, H. A.,Stein, F.,Venekamp, J. C.
, p. 181 - 186 (2007/10/02)
Electrochemical oxidation of 2,4:3,5-di-O-methylene-D-gluconic acid in strong alkaline medium afforded a mixture of 2,4:3,5-di-O-methylene-D-glucaric acid 4 and 2,4:3,5-di-O-methylene-L-idaric acid 1 in a 1/8 ratio with a current efficiency of 53percent.Force-field calculations using Allinger's molecular mechanics program MM2p85 on 1 and 4 indicate that these cis-fused tetrahydro-dioxino-1,3-dioxin ring systems possess an O-inside conformation with a steric energy of 110.3 and 123.5 kJ*mol-1, respectively.Their conformation was confirmed by 400-MHz 1H- and 100-MHz 13C NMR measurements.A series of polycondensates were prepared by homogeneous solution polymerisation of 1 with an aromatic diol or aromatic diamine, which were analyzed by DSC and TGA.
SYNTHESIS OF L-IDARO-1,4-LACTONE, AN INHIBITOR OF α-L-IDOSID-URONASE
Herd, J. Kenneth,Mayberry, William R.,Snell, Robert L.
, p. 33 - 40 (2007/10/02)
L-Idaro-1,4-lactone was synthesized by two different, published methods: (1) epimerization of monopotassium D-glucarate by refluxing in aqueous barium hydroxide, and (2) oxidation of L-iditol by heating in dilute nitric acid.The lactone, formed by heat dehydration from aqueous solution at low pH, was purified by paper chromatography, and quantitated by gas-liquid chromatography using inositol as the internal standard.The monolactone inhibited human, seminal-fluid α-L-idosiduronase activity, with either phenyl or 4-methylumbelliferyl α-L-idosiduronic acid as the substrate, to the same degree as D-glucaro-1,4-lactone inhibits α-D-glucosiduranose.
