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Cis-2,5-bis(hydroxymethyl)-tetrahydrofuran ditosylate is a complex organic chemical compound with the molecular formula C12H16O8S2. It is derived from tetrahydrofuran, a cyclic ether, by substituting two hydrogen atoms with hydroxymethyl groups and then reacting with tosyl chloride to form the ditosylate ester. cis-2,5-bis(hydroxymethyl)-tetrahydrofuran ditosylate is characterized by its cis-configuration, which refers to the arrangement of the hydroxymethyl groups on the same side of the tetrahydrofuran ring. It is a colorless, crystalline solid that is soluble in organic solvents. Due to its unique structure and reactivity, cis-2,5-bis(hydroxymethyl)-tetrahydrofuran ditosylate has potential applications in organic synthesis, particularly in the formation of complex molecules and the protection of functional groups.

1472-00-0

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1472-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1472-00-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1472-00:
(6*1)+(5*4)+(4*7)+(3*2)+(2*0)+(1*0)=60
60 % 10 = 0
So 1472-00-0 is a valid CAS Registry Number.

1472-00-0Relevant articles and documents

3-(5-HYDROXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF

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Paragraph 1390-1391, (2020/02/05)

The present disclosure provides a compound of Formula (I′): or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein Rx, X1, X2, and R1 are as defined herein, and methods of making and using same.

SYNTHESIS OF DIACIDS, DIALDEHYDES, OR DIAMINES FROM THF-DIOLS

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Page/Page column 10; 11, (2015/05/05)

A simple and elegant chemical process for the synthesis of oxygenated products, such as acids and aldehydes, or other derivative products, such as amines and nitriles, of cyclic bifunctional molecules made from renewable, bio-based sources such as HMF and

THIENOPYRIMIDINE AND PYRAZOLOPYRIMIDINE COMPOUNDS AND THEIR USE AS MTOR KINASE AND PI3 KINASE INHIBITORS

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Page/Page column 63, (2009/04/24)

The invention relates to thienopyrimidine and pyrazolopyrimidine compounds of the Formulas (Ia) and (IIa), or a pharmaceutically acceptable salt thereof, wherein the constituent variables are as defined herein compositions comprising the compounds, and methods for making and using the compounds.

Catalytic hydrogenation of 5-hydroxymethylfurfural in aqueous medium

Schiavo, V.,Descotes, G.,Mentech, J.

, p. 704 - 711 (2007/10/02)

The catalytic hydrogenation of 5-hydroxymethylfurfural (HMF) in aqueous medium was studied in presence of Ni, Cu, Pt, Pd, Ru based catalysts.In neutral aqueous mdeium, two major products are abtained in very good yields: 2,5-bis-hydroxymethylfuran (Cu, Pt, Ru) and 2,5-bis-hydroxymethyltetrahydrofuran-cis (Ni, Pd, Ru).In acidic aqueous medium, hydrogenolysis reactions occur and the hydrogenation of HMF leads to two other products: 1-hydroxyhexane-2,5-dione and hexane-1,2,5-triol, mainly in presence of Pt and Ru.A mechanism of formation of these two compounds is proposed.Key words: 5-hydroxymethylfurfural / hydrogenation / hydrogenolysis

Synthesis of Stereoisomeric Crown Ethers Composed of cis- and trans-2,5-Bis(hydroxymethyl)tetrahydrofuran Units and Their Selective Transport of Alkali Metal Cations through Liquid Membranes

Nakazaki, Masao,Naemura, Koichiro,Makimura, Masaru,Matsuda, Atsushi,Kawano, Takaaki,Ohta, Yoshihiro

, p. 2429 - 2435 (2007/10/02)

Optical resolution of trans-tetrahydrofuran-2,5-dicarboxylic acid (13) was carried out via the (+)-2-(1-aminoethyl)naphthalene salt, and conversion of the (+) enantiomer 13 into (+)-2,5-dimethyltetrahydrofuran (17) of known configuration established its 2R,5R configuration.Condensation of (+)- and (-)-trans-ditosylates 15 and cis-ditosylate 20 with pyrocatechol afforded (-)-D2-trans,trans-8, (-)-C1-cis,trans-9, meso-C2h-trans,trans-10, and a mixture of meso-C2h-11 and meso-C2v-cis,cis crown ethers 12.Their selective transport of alkali metal cations is reported.

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