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FUMARALDEHYDE BIS(DIMETHYL ACETAL), also known as FDMA, is a clear colorless to slightly yellow liquid with unique chemical properties. It is an organic compound that plays a significant role in various chemical syntheses and industrial applications due to its versatile chemical structure.

6068-62-8

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6068-62-8 Usage

Uses

Used in Chemical Synthesis:
FUMARALDEHYDE BIS(DIMETHYL ACETAL) is used as an intermediate in the chemical synthesis process for the production of C20-carotene and crocetin or descrocetin esters. Its unique structure allows for the creation of these important compounds, which have various applications in the pharmaceutical, cosmetic, and food industries.
Used in the Preparation of Fumaraldehyde Dimethylacetal (FDMA):
FUMARALDEHYDE BIS(DIMETHYL ACETAL) is also used as a starting material in the preparation of fumaraldehyde dimethylacetal (FDMA) through partial acid hydrolysis. FDMA is an essential compound in various industrial applications, including the production of resins, plastics, and other synthetic materials.

Purification Methods

Dry it over fused CaCl2 and distil it in vacuo. The maleic (cis) isomer has b 112o/11mm, and d23 0.932 and n 251.4243. [Zeik & Heusner Chem Ber 90 1869 1957, Clauson-Kaas et al. Acta Chem Scand 9 111 1955, Clauson-Kaas Acta Chem Scand 6 569 1952, Beilstein 1 IV 3754.]

Check Digit Verification of cas no

The CAS Registry Mumber 6068-62-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6068-62:
(6*6)+(5*0)+(4*6)+(3*8)+(2*6)+(1*2)=98
98 % 10 = 8
So 6068-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O4/c1-9-7(10-2)5-6-8(11-3)12-4/h5-8H,1-4H3/b6-5+

6068-62-8 Well-known Company Product Price

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  • Aldrich

  • (368202)  Fumaraldehydebis(dimethylacetal)  95%

  • 6068-62-8

  • 368202-5G

  • 1,625.13CNY

  • Detail
  • Aldrich

  • (368202)  Fumaraldehydebis(dimethylacetal)  95%

  • 6068-62-8

  • 368202-25G

  • 5,153.85CNY

  • Detail

6068-62-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Fumaraldehyde bis(dimethylacetal)

1.2 Other means of identification

Product number -
Other names (E)-1,1,4,4-tetramethoxybut-2-ene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6068-62-8 SDS

6068-62-8Relevant articles and documents

Total Synthesis of a Docosahexaenoic Acid Prostanoid Using an Intramolecular Organocatalytic Michael Reaction of a Formyl-Enal Derivative

Bultel-Poncé, Valérie,Durand, Thierry,Galano, Jean-Marie,Guy, Alexandre,Oger, Camille,Revol-Cavalier, Johanna

supporting information, p. 7455 - 7459 (2020/10/09)

The total synthesis of a docosahexaenoic-acid-derived prostaglandin, 4,11-diepi-4-F4t-neuroprostane, featuring a complex lateral chain was achieved for the first time. A novel prostaglandin cyclopentane skeleton obtained via an intramolecular highly selective organocatalytic Michael sequence of a formyl-enal derivative allowed the desired and exclusive thermodynamic trans configuration of the lipidic lateral chains.

BIPOLAR TRANS CAROTENOID SALTS AND USES THEREOF

-

Paragraph 0083; 0095; 0116; 0117, (2018/10/26)

PROBLEM TO BE SOLVED: To provide compounds useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans. SOLUTION: There is provided a compound which has a structure represented by YZ-TCRO-ZY and is not trans sodium crocetinate [where, Y is a cation; Z is a polar group which is associated with the cation; and TCRO is trans carotenoid skeleton], and preferably, Y is a monovalent metal ion selected from the group consisting of Na+, K+ and Li+, or is an organic cation selected from the group consisting of R4 N+ and R3S+ [R is H, or CnH2n+1(n is 1 to 10)]. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPO&INPIT

Synthesis of a simplified triazole analogue of pateamine A

Hemi Cumming,Brown, Sarah L.,Tao, Xu,Cuyamendous, Claire,Field, Jessica J.,Miller, John H.,Harvey, Joanne E.,Teesdale-Spittle, Paul H.

, p. 5117 - 5127 (2016/06/14)

Pateamine A is a naturally occurring metabolite extracted from the marine sponge Mycale hentscheli. It exhibits potent cytotoxicity towards cancer cell lines and has been shown to target protein translation initiation via inhibition of the function of euk

BIPOLAR TRANS CAROTENOID SALTS AND THEIR USE

-

Paragraph 0095; 0116-0117, (2018/10/31)

PROBLEM TO BE SOLVED: To provide trans carotenoid salt compounds useful for improving the diffusibility of oxygen between red blood cells and a body tissue in mammalian including human being, a method for producing them, a method for solubilizing them, and a method for using them. SOLUTION: There are provided compounds represented by the following formula, and are compounds not being trans sodium crocetinate: YZ-TCRO-ZY[Y denotes a cation; Z denotes a polar group coupled to the cation; TCRO denotes a trans carotenoid skeleton; preferably, as follows; Y denotes the monovalent metal ion of Na+,K+ or Li+ or R4 N+ or R3S+;R denotes H or CnH2n+1;n denotes the integer of 1 to 10;Z denotes a carboxyl group, a sulfuric acid group, a mono-phosphoric acid group, a di-phosphoric acid group, or a tri-phosphoric acid group; and TCRO denotes a group using isopronoid in which the single bond and double bond of straight chain carbon and carbon as exemplified by the following formula is repeated (X respectively independently denotes H, a straight chain/branched carbon chain substituted/non-substituted with 1 to 10C halogen or a halogen)]. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPO&INPIT

Stereoselective synthesis of epoxyisoprostanes: an organocatalytic and "pot-economy" approach

Weng, Jiang,Wang, Sheng,Huang, Lin-Jie,Luo, Zhang-Yi,Lu, Gui

supporting information, p. 10170 - 10173 (2015/06/22)

An efficient and direct synthetic route to epoxyisoprostane EC methyl ester has been accomplished in 8 steps (10% overall yield) from readily available starting materials using a series of asymmetric organocatalytic reactions and one-pot operations.

BIPOLAR TRANS CAROTENOID SALTS AND THEIR USES

-

Page/Page column 26, (2008/06/13)

The invention relates to trans carotenoid salt compounds, methods for making them, methods for solubilizing them and uses thereof. These compounds are useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans.

Bipolar trans carotenoid salts and their uses

-

Page 8; 10-11, (2008/06/13)

The invention relates to trans carotenoid salt compounds, methods for making them, methods for solubilizing them and uses thereof. These compounds are useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans.

A Short and Efficient Synthesis of Crocetin-dimethylester and Crocetindial

Frederico, Daniel,Marcos Donate, Paulo,Gomes Constantino, Mauricio,Soares Bronze, Erika,Sairre, Mirela I.

, p. 9126 - 9128 (2007/10/03)

In this paper we describe an efficient six-step synthesis of crocetin-dimethylester that could be further reduced to a "four-step" synthesis through the use of in situ procedures. The simplicity of the whole process, the ready availability of starting materials, and the high overall yield render this strategy a very attractive synthesis of this very important compound, which is the key intermediate for the synthesis of several carotenoids and other polyene natural products.

Preparation of 1,1,4,4-tetramethoxy-2-butene

-

Page column 5-6, (2010/02/05)

A process for the preparation of 1,1,4,4-tetramethoxy-2-butene by reacting 2,5-dimethoxydihydrofuran with methanol in the presence of acids comprises carrying out the reaction in the presence of solid catalysts having acidic centers.

Stereocontrolled preparation of the C1-C14 polyene fragment of benzenic ansamycin antibiotics ansatrienin A and B

Sch?ning, Kai-Uwe,Wittenberg, Rüdiger,Kirschning, Andreas

, p. 1624 - 1626 (2007/10/03)

A practical synthesis of the C1-C14 polyene unit 5 in ansatrienin A (mycotrien l), 1a, and other ansamycin antibiotics is described which involves elaboration of the chiral unsaturated aldehyde 6 and phosphonate 7, followed by coupling of the building blocks by Horner-Emmons-olefination and Duthaler's aldolation. The synthesis of 6 successfully applies two consecutive Evans-aldol reactions for constructing the carbon backbone.

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