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6068-62-8

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6068-62-8 Usage

Chemical Properties

Clear colorless to slightly yellow liquid

Uses

Fumaraldehyde bis(dimethyl acetal) may be used in the syntheses of C20-carotene and crocetin or descrocetin esters. It may be used in the preparation of fumaraldehyde dimethylacetal, (FDMA), by partial acid hydrolysis.

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.

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

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.

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