31525-67-4 Usage
Description
4,4-Dimethoxy-2-methyl-2-butanol, also known as 4,4-dimethoxy-2-methyl-2-butanol 97, is an organic compound that serves as a versatile building block in the synthesis of various chemical compounds. It is characterized by its molecular structure, which includes a butanol backbone with two methoxy groups and a methyl group attached to the second carbon.
Uses
Used in Chemical Synthesis:
4,4-Dimethoxy-2-methyl-2-butanol 97 is used as a synthetic building block for the creation of various chemical compounds. Its unique molecular structure allows it to be a valuable component in the synthesis process.
Used in Microwave-Mediated Synthesis:
In the field of microwave-mediated synthesis, 4,4-dimethoxy-2-methyl-2-butanol 97 is used as a reactant for the synthesis of 2,2-dimethyl-2H-chromones. These chromones are important intermediates in the production of various pharmaceuticals and other chemical products.
Used in the Preparation of DCP Analogs:
4,4-Dimethoxy-2-methyl-2-butanol 97 is also utilized in the preparation of alkyl substituted 3′R,4′R-di-O-(-)-camphanoyl-2′,2′-dimethyldihydropyrano[2,3-f]chromone (DCP) analogs. DCP analogs have potential applications in various fields, including pharmaceuticals and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 31525-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31525-67:
(7*3)+(6*1)+(5*5)+(4*2)+(3*5)+(2*6)+(1*7)=94
94 % 10 = 4
So 31525-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O3/c1-7(2,8)5-6(9-3)10-4/h6,8H,5H2,1-4H3
31525-67-4Relevant articles and documents
Asymmetric Solid-Phase Synthesis of (3′R,4′R)-Di-O-cis-acyl 3-Carboxyl Khellactones
Xia, Yi,Yang, Zheng-Yu,Brossi, Arnold,Lee, Kuo-Hsiung
, p. 2113 - 2115 (1999)
Matrix Presented We describe a practical parallel synthesis of (3′R,4′R)-di-O-cis-acyl 3-carboxyl khellactones on a solid phase in high yield. The highlights of this synthesis include a Knoevenagel condensation, asymmetric dihydroxylation, catalyzed acylation, and product cleavage from the solid support.
Fructose 1,6-Diphosphate Aldolase Catalyzed Stereoselective Synthesis of C-Alkyl and N-Containing Sugars: Thermodynamically Controlled C-C Bond Formations.
Durrwachter, John R.,Wong, Chi-Huey
, p. 4175 - 4181 (2007/10/02)
Fructose 1,6-diphosphate aldolase catalyzed aldol condensations have been used in syntheses of several new N-containing and C-alkyl sugars on 4-20 mmol scales.The enzyme is highly specific for dihydroxyacetone phosphate as donor but accepts a number of achiral and chiral aldehydes (both D and L isomers) as acceptors.Due to the reversible nature of the aldol reaction, a thermodynamically controlled approach was employed for the syntheses in which racemic aldehydes were used as substrates and thermodynamically more stable products were preferentially produced.