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Dimethyl 2-methyl-5-methyleneadipate is a chemical compound with the molecular formula C10H14O4. It is an organic ester derived from 2-methyl-5-methyleneadipate, which is a dicarboxylic acid with a methyl group at the 2nd carbon and a methylene group at the 5th carbon. The compound is formed by the esterification of 2-methyl-5-methyleneadipate with methanol, resulting in the attachment of two methyl groups to the carboxylic acid groups. Dimethyl 2-methyl-5-methyleneadipate is a colorless liquid with a pungent odor and is used in the synthesis of various chemicals, pharmaceuticals, and as a fragrance component in the perfume industry. It is also known for its potential applications in the production of polymers and as a precursor in the synthesis of other complex organic molecules.

4513-62-6

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4513-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4513-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4513-62:
(6*4)+(5*5)+(4*1)+(3*3)+(2*6)+(1*2)=76
76 % 10 = 6
So 4513-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O4/c1-7(9(11)13-3)5-6-8(2)10(12)14-4/h8H,1,5-6H2,2-4H3

4513-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-methyl-5-methylidenehexanedioate

1.2 Other means of identification

Product number -
Other names 2-Methyl-5-methylen-adipinsaeure-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:4513-62-6 SDS

4513-62-6Relevant academic research and scientific papers

Thermal Degradation of Polymers and Polymer Models.IV. Thermolysis of a Polymethacrylate Model with an Unsaturated End Group

Morrow, Gregory R.,Rae, Ian D.

, p. 1477 - 1481 (1987)

Thermal Degradation of a model for the 'unsaturated end group' of poly(methyl methacrylate) gives products which suggest that homolytic bond cleavage, and not a retro-ene reaction, is the major pathway.The diester (CH3)2C(COOCH3)CH2C(COOCH3)=CH2, when heated at 250/300 deg, gives up to 50 mole percent of methyl 2-methylpropanoate (methyl isobutyrate).

Cyclodextrin-centred star polymers synthesized via a combination of thiol-ene click and ring opening polymerization

Zhang, Qiang,Li, Guang-Zhao,Becer, C. Remzi,Haddleton, David M.

supporting information; experimental part, p. 8063 - 8065 (2012/09/07)

The synthesis of cyclodextrin-centred star polymers via thiol-ene addition of per-6-thio-β-cyclodextrin (CD-(SH)7) with vinyl terminated polymers is described. The obtained thiol-ene product was employed as an initiator for ring opening polymerization (ROP) of ε-caprolactone (ε-CL).

Catalytic tail-to-tail selective dimerization of methyl methacrylate promoted by a ruthenium(0) complex

Hirano, Masafumi,Hiroi, Yuki,Komine, Nobuyuki,Komiya, Sanshiro

scheme or table, p. 3690 - 3693 (2010/12/20)

Ru(η6-naphthalene)(η4-1,5-COD) (1) (10 mol %) catalyzes the tail-to-tail dimerization of methyl methacrylate (MMA) in MeCN in 74% yield at 70 °C for 4 h. Without use of solvent complex 1 (1 mol %) rapidly catalyzes the tail-to-tail dimerization and trimerization of MMA in 59% and 23% yields, respectively, at 70 °C for 5 min.

Thermal Cross-coupled Dimerisation of Alkali and Alkaline Earth Metal Salts of Methacrylic-Crotonic Acid Binary Systems in the Solid State

Kudoh, Masaaki,Naruchi, Kiyoshi,Akutsu, Fumihiko,Miura, Masatoshi

, p. 105 - 106 (2007/10/02)

Thermal reaction of sodium and potassium salts of methacrylic-crotonic acids in the solid state selectively affords a cross-coupled dimer, dimethyl hex-1-ene-2,4-dicarboxylate.

On the Catalytic Dimerization of Acrylic Acid Derivatives by Palladium Complexes. IV. The Dimerization of Methyl Methacrylate

Oehme, G.

, p. 779 - 790 (2007/10/02)

Methyl methacrylate has been dimerized to a mixture of 2.5-di(methoxycarbonyl)-hex-1-ene (1) and (E)-2.5-di(methoxycarbonyl)-hex-2-ene (2) by catalytic systems containing dichlorobis (nitrile)-palladium(II) and silver tetrafluoroborate.Codimerization experiments with methyl acrylate show a lower reactivity of methyl methacrylate.Oxidative addition of β-chloro methyl methacrylate to tetrakis(triphenylphosphine)palladium(0) gave β-palladio methyl methacrylates (8,9) suitable for model investigations of the catalytic reaction.A proposal is given for a mechanism via Pd(IV) intermediates.

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