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32251-35-7

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  • 1,14-DIMETHYL-4,10-DIOXATETRACYCLO[5.5.2.0(2,6).0(8,12)]TETRADEC-13-ENE-3,5,9,11-TETRAONE

    Cas No: 32251-35-7

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32251-35-7 Usage

Description

1,14-DIMETHYL-4,10-DIOXATETRACYCLO[5.5.2.0(2,6).0(8,12)]TETRADEC-13-ENE-3,5,9,11-TETRAONE is a complex organic compound characterized by its tetracyclic structure and multiple oxygen atoms. As a cyclic ether derivative, it features four ketone functional groups. This intricate molecular structure presents challenges in synthesis and study, yet it holds promise for applications in organic chemistry and pharmaceuticals. Further research is essential to comprehend its full potential and properties.

Uses

Used in Organic Chemistry:
1,14-DIMETHYL-4,10-DIOXATETRACYCLO[5.5.2.0(2,6).0(8,12)]TETRADEC-13-ENE-3,5,9,11-TETRAONE is used as a key intermediate for the synthesis of various complex organic molecules due to its unique tetracyclic structure and multiple functional groups.
Used in Pharmaceutical Industry:
1,14-DIMETHYL-4,10-DIOXATETRACYCLO[5.5.2.0(2,6).0(8,12)]TETRADEC-13-ENE-3,5,9,11-TETRAONE is used as a potential pharmaceutical candidate for the development of new drugs, given its complex structure and the presence of multiple oxygen atoms, which may offer novel interactions with biological targets.
Used in Material Science:
1,14-DIMETHYL-4,10-DIOXATETRACYCLO[5.5.2.0(2,6).0(8,12)]TETRADEC-13-ENE-3,5,9,11-TETRAONE may be used as a component in the development of advanced materials, such as polymers or composites, due to its unique structural properties and potential for molecular engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 32251-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,5 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32251-35:
(7*3)+(6*2)+(5*2)+(4*5)+(3*1)+(2*3)+(1*5)=77
77 % 10 = 7
So 32251-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O6/c1-4-3-14(2)8-6(10(15)19-12(8)17)5(4)7-9(14)13(18)20-11(7)16/h3,5-9H,1-2H3

32251-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 32251-35-7

1.2 Other means of identification

Product number -
Other names (+-)-1,8-Dimethyl-bicyclo[2.2.2]oct-7-en-2exo,3exo,5exo,6exo-tetracarbonsaeure-2,3,5,6-dianhydrid

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:32251-35-7 SDS

32251-35-7Relevant articles and documents

Multicomponent reaction of aldehydes, anhydrides, and dienophiles: Synthesis of butterfly -like diazatetradecenes

Struebing, Dirk,Von Wangelin, Axel Jacobi,Neumann, Helfried,Goerdes, Dirk,Huebner, Sandra,Klaus, Stefan,Spannenberg, Anke,Beller, Matthias

, p. 107 - 113 (2007/10/03)

An operationally simple one-pot synthesis of functionalized bicyclo[2.2.2]oct-2-ene derivatives has been developed using a novel multicomponent coupling of α,β-unsaturated aldehydes, carboxylic acid anhydrides, and dienophiles. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.

Diels-Alder Reactions of Cyclohexadienes Derived from Decarboxylation of Photocycloadducts between 4,6-Dimethyl-2-pyrone and Cyclic Olefins

Shimo, Tetsuro,Matsuo, Kenji,Somekawa, Kenichi,Tsuge, Otohiko

, p. 549 - 551 (2007/10/02)

Labile photo adducts between 4,6-dimethyl-2-pyrone and cyclic olefins reacted with second olefins to give cross adducts, and with acetylenes to afford both bis-adducts and benzene derivatives with the concurrent decarboxylation, respectively.The rea

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