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10260-41-0

Tetrahydro-2,5-furandicarboxylic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10260-41-0 Structure

  • Basic information

    1. Product Name: Tetrahydro-2,5-furandicarboxylic acid dimethyl ester
    2. Synonyms: Tetrahydro-2,5-furandicarboxylic acid dimethyl ester
    3. CAS NO:10260-41-0
    4. Molecular Formula:
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10260-41-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Tetrahydro-2,5-furandicarboxylic acid dimethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Tetrahydro-2,5-furandicarboxylic acid dimethyl ester(10260-41-0)
    11. EPA Substance Registry System: Tetrahydro-2,5-furandicarboxylic acid dimethyl ester(10260-41-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10260-41-0(Hazardous Substances Data)

10260-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10260-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,6 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10260-41:
(7*1)+(6*0)+(5*2)+(4*6)+(3*0)+(2*4)+(1*1)=50
50 % 10 = 0
So 10260-41-0 is a valid CAS Registry Number.

10260-41-0Relevant articles and documents

Tetrahydrofuran derivatives and their use as plasticizers

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, (2016/10/10)

The present invention relates to tetrahydrofuran derivatives, a plasticizer composition containing said tetrahydrofuran derivatives, molding materials containing a thermoplastic polymer and such a tetrahydrofuran derivative, to a process for the production of these tetrahydrofuran derivatives and their use.

TETRAHYDROFURAN DERIVATIVES AND USE THEREOF AS PLASTICIZERS

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Paragraph 0251, (2016/04/09)

The invention relates to tetrahydrofuran derivatives of general formula (I), wherein X stands for *—(C═O)—O—, *—(CH2)n-O—, or *—(CH2)n-O—(C═O)—, wherein * represents the point of bonding to the tetrahydrofuran ring and n has the value 0, 1, or 2; and R1 and R2 are selected independently of each other from among C4-C5 alkyl and C5-C6 cycloalkyl, wherein the cycloalkyl groups are unsubstituted or can be substituted by at least one C1-C10 alkyl group, a plasticizer composition that contains said tetrahydrofuran derivatives, molding masses that contain a thermoplastic polymer or an elastomer and such a tetrahydrofuran derivative. The invention further relates to a method for producing said tetrahydrofuran derivatives, and to the use of said tetrahydrofuran derivatives

TETRAHYDROFURAN DERIVATIVES AND USE THEREOF AS PLASTICIZERS

-

, (2016/10/10)

A method and apparatus for hybrid multi-layer transmission includes receiving a multi-layer signal from a source device, wherein the multi-layer signal includes a plurality of sublayers. A quantity of the plurality of sublayers is decoded and partial information relating to the decoded sublayers is transmitted to a destination device.

Enzymes in organic synthesis. 33. Stereoselective pig liver esterase-catalyzed hydrolyses of meso cyclopentyl-, tetrahydrofuranyl-, and tetrahydrothiophenyl-1,3-diesters

Jones, J. Bryan,Hinks, R. Scott,Hultin, Philip G.

, p. 452 - 456 (2007/10/02)

Preparative-scale pig liver esterase-catalyzed hydrolyses of five-membered ring meso-1,3-diesters are enantiotopically selective.While pro-S enantiotopic selectivity is exhibited in each case, the absolute configuration sense of the hydrolysis in the cyclopentyl series is opposite to that of both the tetrahydrofuranyl and tetrahydrothiophenyl diesters.The enantiomeric excess levels induced are in the 34-46percent range.

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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