Pharmaceutical Intermediates 2,5-Dimethoxytetrahydrofuran 696-59-3 Good Manufacturer

Product Details

Quick Details

CasNo： 696-59-3
Molecular Formula： C₆H₁₂O₃
Appearance： Colorless to light yellow liquid
Purity： 99%

Pharmaceutical Intermediates 2,5-Dimethoxytetrahydrofuran 696-59-3 Good Manufacturer

696-59-3 Name
Name	2,5-Dimethoxytetrahydrofuran
Synonym	2,5-Dimethoxytetrahydrofuran,c&t;tetrahydro-2,5-dimethoxy-fura;DMTHF;DIMETHOXYTETRAHYDROFURAN;FURAN, TETRAHYDRO-2,5-DIMETHOXY;2,5-DIMETHOXYTETRAHYDROFURAN;2,5-Dimethoxytetrahydrofuran, mixture of cis and trans;2,5-DIMETHOXY-TETRAHYDROFURAN (CIS+TRANS )

696-59-3 Chemical & Physical Properties
Melting point	-45 °C
Boiling point	145.7±0.0 °C at 760 mmHg
Density	1.0±0.1 g/cm3
Molecular Formula	C6H12O3
Molecular Weight	132.158
Flash Point	35.0±0.0 °C
PSA	27.69000
LogP	-0.83
Exact Mass	132.078644
Vapour Pressure	6.1±0.2 mmHg at 25°C
Index of Refraction	1.423
Storage condition	Flammables area
Water Solubility	350 g/L (20 ºC)

Pharmaceutical Intermediates 2,5-Dimethoxytetrahydrofuran 696-59-3 Usage

2,5-Dimethoxytetrahydrofuran is a chemical compound that has been studied in various scholarly articles for its potential applications as a pharmaceutical intermediate. It can be used as a starting material for the synthesis of various pharmaceuticals, such as antihypertensive and antitumor agents. Additionally, 2,5-Dimethoxytetrahydrofuran has been investigated for its potential applications as a solvent and reagent in organic synthesis. It has been found to have high solubility in various organic solvents and can be used in reactions such as oxidation, reduction, and cyclization. Furthermore, 2,5-Dimethoxytetrahydrofuran has been studied for its potential applications in the production of polymers and resins. However, it is important to note that 2,5-Dimethoxytetrahydrofuran is a hazardous chemical and should be handled with care.

InChI:InChI=1/C6H12O3/c1-7-5-3-4-6(8-2)9-5/h5-6H,3-4H2,1-2H3/t5-,6+

696-59-3 Relevant articles

Photographic emulsions containing 2, 5-dimethoxytetrahydrofuran

Alexander, Stanton William

, US13581949A (02/12/1952)

Linkers for the synthesis of multiple oligonucleotides in seriatim from a single support attachment

-

, (2008/06/13)

A method for the synthesis of a plurality of oligonucleotides comprising the steps of (i) forming a first oligonucleotide on a first cleavable link attached to a solid support; (ii) attaching to the first oligonucleotide a cleavable linker moiety; (iii) forming a second oligonucleotide on the cleavable linker moiety; and (iv) cleaving the first cleavable link and the cleavable linker moiety to give a plurality of oligonucleotides; wherein the cleavable linker moiety is of the Formula (1): STR1 in which A1, A2 and E are as defined herein, and novel compounds which may be used in the operation of the method.

Agrochemical compositions and methods employing hymexazol and 1,2-benzisothiazolin-3-one

-

, (2008/06/13)

A combination of 3-hydroxy-5-methylisoxazole with an antimicrobial agent has good agricultural fungicidal activity which lasts longer than 3-hydroxy-5-methylisoxazole alone. The dihydrate of the calcium salt of 3-hydroxy-5-methylisoxazole has advantages over the free 3-hydroxy-5-methylisoxazole, other salts and the anhydrous compound.

Difunctional and Hetercyclic Prducts from the Ozonolysis of Conjugated C5-C8 Cyclodienes

Griesbaum, Karl,Jung, In Chang,Mertens, Henri

, p. 6024 - 6027 (2007/10/02)

Ozonolyses of the conjugated C5-C8 cyclodienes 1a-d in methanol, followed by reduction with DMS, have been examined.Monoozonolyses gave the corresponding unsaturated dialdehydes 2e as the primary products.In subsequent reactions, the dialdehydes 2e derived from the monoozonolyses of 1a, 1b, and 1c gave in high yields the heterocyclic compounds 7, 8k, and 9k, respectively.Diozonolyses of 1a-d gave the corresponding dialdehydes 3e as the primary products.In subsequent reactions, the dialdehydes 3e derived from 1b and 1c gave the heterocyclic compounds 8l and 9l, respectively.In addition, aldehydes 2e and 3e undervent partial acetalization reactions with methanol.