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4883-40-3

4-Cyclohexene-1,2-dicarboxylic acid, 4-methyl-, dimethyl ester, cis- is a chemical compound with the molecular formula C10H14O4. It is a derivative of cyclohexene, featuring a cyclohexene ring with two carboxyl groups at the 1 and 2 positions, and a methyl group at the 4 position. The compound is an ester, with two methyl ester groups attached to the carboxyl groups. The cis- configuration indicates that the two methyl ester groups are on the same side of the cyclohexene ring. 4-Cyclohexene-1,2-dicarboxylic acid, 4-methyl-, dimethyl ester, cis- is used in various chemical reactions and as an intermediate in the synthesis of other organic compounds. It is important to note that the compound's properties, such as solubility and reactivity, can be influenced by its stereochemistry, which in this case is the cis- configuration.

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  • 4-Cyclohexene-1,2-dicarboxylic acid, 4-methyl-, dimethyl ester, cis-

    Cas No: 4883-40-3

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  • 4883-40-3 Structure

  • Basic information

    1. Product Name: 4-Cyclohexene-1,2-dicarboxylic acid, 4-methyl-, dimethyl ester, cis-
    2. Synonyms:
    3. CAS NO:4883-40-3
    4. Molecular Formula: C11H16O4
    5. Molecular Weight: 212.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4883-40-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Cyclohexene-1,2-dicarboxylic acid, 4-methyl-, dimethyl ester, cis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Cyclohexene-1,2-dicarboxylic acid, 4-methyl-, dimethyl ester, cis-(4883-40-3)
    11. EPA Substance Registry System: 4-Cyclohexene-1,2-dicarboxylic acid, 4-methyl-, dimethyl ester, cis-(4883-40-3)

  • 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: 4883-40-3(Hazardous Substances Data)

4883-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4883-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4883-40:
(6*4)+(5*8)+(4*8)+(3*3)+(2*4)+(1*0)=113
113 % 10 = 3
So 4883-40-3 is a valid CAS Registry Number.

4883-40-3SDS

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 (+/-)-cis-4-methyl-cyclohex-4-ene-1,2-dicarboxylic acid dimethyl ester

1.2 Other means of identification

Product number -
Other names (+/-)-cis-4-Methyl-cyclohex-4-en-1,2-dicarbonsaeure-dimethylester

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:4883-40-3 SDS

4883-40-3Relevant articles and documents

Highly-functionalized arene synthesis based on palladium on carbon-catalyzed aqueous dehydrogenation of cyclohexadienes and cyclohexenes

Yasukawa, Naoki,Yokoyama, Hiroki,Masuda, Masahiro,Monguchi, Yasunari,Sajiki, Hironao,Sawama, Yoshinari

supporting information, p. 1213 - 1217 (2018/03/28)

Transition metal-catalyzed dehydrogenation is a clean oxidation method requiring no additional oxidants. We have accomplished a heterogeneous Pd/C-catalyzed aqueous dehydrogenation of 1,4-cyclohexadienes and cyclohexenes to give the corresponding highly-functionalized arenes. Furthermore, various arenes could be efficiently constructed in a one-pot manner via a Diels-Alder reaction and the following dehydrogenation.

Solvate Ionic Liquids as Reaction Media for Electrocyclic Transformations

Eyckens, Daniel J.,Champion, Megan E.,Fox, Bronwyn L.,Yoganantharajah, Prusothman,Gibert, Yann,Welton, Tom,Henderson, Luke C.

supporting information, p. 913 - 917 (2016/03/01)

Solvate ionic liquids (SILs) consisting of lithium bis(trifluoromethylsulfonyl)imide dissolved in tri-or tetraglyme have recently emerged as a novel class of ionic liquids. Herein, the first use of solvate ionic liquids as a replacement for molecular solvents in electrocyclization reactions is reported. The SILs promoted both Diels-Alder and [2+2] cycloaddition reactions, compared to an appropriate molecular solvent, and 5 M lithium perchlorate in diethyl ether. The Gutmann acceptor number (AN) of these solvate ionic liquids has also been determined by 31P NMR spectroscopy to be 26.5, thus being modest Lewis acids.

Syntheses of isomerically pure reference octalins and hydrindanes

Lee, Jun Hee,Kim, Woo Han,Danishefsky, Samuel J.

supporting information; experimental part, p. 5482 - 5484 (2010/01/18)

We describe herein the development of efficient and stereoselective synthetic routes to a range of cis- and trans-octalin and hydrindane target compounds.

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