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Cyclohexane-1,4-diyldimethanediyl diacetate is a complex organic compound with the chemical formula C14H20O4. It is a white crystalline solid that is soluble in organic solvents. cyclohexane-1,4-diyldimethanediyl diacetate is derived from cyclohexane, a cyclic hydrocarbon, and features a diacetate group, which means it has two acetate groups attached to a central cyclohexane ring through methylene bridges. The compound is used in the synthesis of various polymers and resins, particularly in the production of polyurethanes and polycarbonates, due to its ability to form strong, stable bonds. It is also known for its potential applications in the pharmaceutical industry and as a chemical intermediate in the synthesis of other complex molecules. The compound's properties, such as its molecular structure and reactivity, make it a valuable component in the creation of durable and versatile materials.

6308-18-5

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6308-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6308-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6308-18:
(6*6)+(5*3)+(4*0)+(3*8)+(2*1)+(1*8)=85
85 % 10 = 5
So 6308-18-5 is a valid CAS Registry Number.

6308-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(acetyloxymethyl)cyclohexyl]methyl acetate

1.2 Other means of identification

Product number -
Other names 1,4-cyclohexanedimethylene diacetate

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:6308-18-5 SDS

6308-18-5Relevant academic research and scientific papers

Extended Release of Native Drug Conjugated in Polyketal Microparticles

Guo, Shutao,Nakagawa, Yoshiyuki,Barhoumi, Aoune,Wang, Weiping,Zhan, Changyou,Tong, Rong,Santamaria, Claudia,Kohane, Daniel S.

, p. 6127 - 6130 (2016)

Polyketals, which can be biodegradable, have good biocompatibility, and are pH-sensitive, could have broad applicability in drug delivery and other biomedical applications. However, facile synthesis of high molecular weight polyketals is challenging, and

Dehydrogenative ester synthesis from enol ethers and water with a ruthenium complex catalyzing two reactions in synergy

Kar, Sayan,Luo, Jie,Rauch, Michael,Diskin-Posner, Yael,Ben-David, Yehoshoa,Milstein, David

supporting information, p. 1481 - 1487 (2022/03/07)

We report the dehydrogenative synthesis of esters from enol ethers using water as the formal oxidant, catalyzed by a newly developed ruthenium acridine-based PNP(Ph)-type complex. Mechanistic experiments and density functional theory (DFT) studies suggest that an inner-sphere stepwise coupled reaction pathway is operational instead of a more intuitive outer-sphere tandem hydration-dehydrogenation pathway.

SYNTHESIS OF BICYCLO[2.2.2]OCTANE DERIVATIVES

-

Paragraph 0083, (2019/05/02)

Provided is a process for the preparation of certain 1,4-bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst to afford an oxo-substituted bicyclo[2.2.2]octane species. This intermediate structure can then be further derivatized. The processes of this disclosure thus affords a novel and simplified means for the commercial production of a wide variety of bicyclo[2.2.2]octane derivatives.

SYNTHESIS OF BICYCLO(2.2.2)OCTANES

-

Paragraph 0040, (2018/05/15)

Provided is a process for the preparation of certain 1,4- bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst comprising a palla

Synthesis and characterization of polycarbonates by melt phase interchange reactions of alkylene and arylene diacetates with alkylene and arylene diphenyl dicarbonates

Sweileh, Bassam A.,Al-Hiari, Yusuf M.,Kailani, Mohammad H.,Mohammad, Hani A.

experimental part, p. 3661 - 3682 (2010/09/08)

This work presents a new synthetic approach to aromatic and aliphatic polycarbonates by melt polycondensation of bisphenol A diacetates with alkylene- and arylenediphenyl dicarbonates. The diphenyl dicarbonates were prepared from phenyl chloroformate and

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