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3-Cyclohexene-1-carboxylic acid, 4-(4-methyl-3-pentenyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53311-89-0

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53311-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53311-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,1 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53311-89:
(7*5)+(6*3)+(5*3)+(4*1)+(3*1)+(2*8)+(1*9)=100
100 % 10 = 0
So 53311-89-0 is a valid CAS Registry Number.

53311-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-(4-methylpent-3-enyl)cyclohex-3-ene-1-carboxylate

1.2 Other means of identification

Product number -
Other names 4-(4-Methyl-pent-3-enyl)-cyclohex-3-encarbonsaeure-methylester

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:53311-89-0 SDS

53311-89-0Relevant academic research and scientific papers

USE OF COMPOSITIONS OBTAINED BY CALCINING PARTICULAR METAL-ACCUMULATING PLANTS FOR IMPLEMENTING CATALYTICAL REACTIONS

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Paragraph 0871, (2016/01/25)

The use of metal-accumulating plants for implementing chemical reactions especially catalytical reactions.

Surfactants and Solvents Containing Diels-Alder Adducts

-

Page/Page column 3, (2015/02/18)

Surfactants and solvents containing derivatized adducts formed from Diels-Alder reactions of terpenes and unsaturated carboxylic acids or their derivatives are disclosed. Processes for making and derivatizing the Diels-Alder adducts are also disclosed.

Preparation of ecological catalysts derived from Zn hyperaccumulating plants and their catalytic activity in Diels-Alder reaction

Escande, Vincent,Olszewski, Tomasz K.,Grison, Claude

, p. 731 - 737 (2014/07/21)

Zn hyperaccumulating plants Noccaea caerulescens and Anthyllis vulneraria were used as the starting material for preparation of novel Lewis ecological catalysts. Those catalysts efficiently mediate the Diels-Alder reaction. High yields, very good regio- a

Ruthenium-catalysed codimerisation of myrcene with methyl acrylate: Catalyst screening and mechanistic discussions

Behr, Arno,Johnen, Leif,Rentmeister, Nils

, p. 204 - 212 (2013/04/10)

The codimerisation of 1,3-dienes and acrylic compounds is a feasible strategy for the synthesis of functionalised alkenes. In this work, a direct approach to novel C13 esters for the flavour and fragrance industry was performed by codimerisatio

High regioselective Diels-Alder reaction of myrcene with acrolein catalyzed by zinc-containing ionic liquids

Yin, Donghong,Li, Changzhi,Li, Biaomo,Tao, Liang,Yin, Dulin

, p. 137 - 142 (2007/10/03)

The ambient zinc-containing ionic liquids, MX-ZnCl2, functioning as both Lewis acid catalyst and green solvent, are employed for a high regioselective Diels-Alder reaction of myrcene with acrolein for the first time, where MX is either 1-butyl-3-methylimidazolium chloride (BmimCl), 1-ethyl-3-methylimidazolium bromide (EmimBr), N-butylpyridinium bromide (BPyBr), or N-ethylpyridinium bromide (EtPyBr). Compared with the analogous reaction performed over a ZnCl2 catalyst in the conventional solvent dichloromethane, higher regioselectivity of the 'para' cycloadduct and excellent yield were achieved at shorter reaction time in these ionic liquids with optimized molar compositions of MX and ZnCl2. These moisture-insensitive ionic liquids can be easily separated from reaction products after simple washing with hexane, allowing their reuse with no obvious loss in activity.

Diels-Alder reaction of myrcene with carbonyl containing dienophiles supported on silica gel under microwave irradiation

Oskooie, Hossein Abdi

, p. 1165 - 1167 (2007/10/03)

Diels-Alder reactions of myrcene (7-methyl-3-methene-1,6-octadiene) with carbonyl containing dienophiles supported on silica gel under microwave irradiation have been studied.

Nanoporous solid acid catalyst for the Diels-Alder reaction of 1,3-dienes with acrylates

Onaka, Makoto,Hashimoto, Naoki,Yamasaki, Ryota,Kitabata, Yasuyoshi

, p. 166 - 167 (2007/10/03)

Nanoporous aluminosilicate, Al-HMS with a high aluminum content, strong acidity, and nanoporosity was found to catalyze the Diels-Alder reaction of 1,3-dienes with methacrylate and acrylate, and turned out to be a green alternative to homogeneous acid catalysts.

DRAMATIC ACCELERATION OF THE DIELS-ALDER REACTION BY ADSORPTION ON CHROMATOGRAPHY ADSORBENTS

Veselovsky, V. V.,Gybin, A. S.,Lozanova, A. V.,Moiseenkov, A. M.,Smit, W. A.,Caple, R.

, p. 175 - 178 (2007/10/02)

The development of a new method for effecting cycloadditions on the surface of chromatographic adsorbents in the absence of solvents that leads to a moderation of the reaction conditions and an increase in selectivity is described.

Synthesis of p-Camphorene

Vig, O. P.,Kad, G. L.

, p. 507 - 509 (2007/10/02)

p-Camphorene is synthesised by the application of Wittig reaction with methylenetriphenylphosphorane on 1(4-methyl-3-pentenyl)-4-(5-methyl-4-hexe-1-one)cyclohex-1-ene (5), the cardinal intermediate, which was procured by the formation of β-ketosulphoxide and then its subsequent alkylation with 1-bromo-3-methyl-2-butene of the compound 1(4-methyl-3-pentenyl)-4-carbmethoxycyclohex-1-ene (3).The alkylated material was submitted to reductive cleavage with aluminium amalgam in aqueous THF at 65 deg to furnish 5.

LINEAR CODIMERIZATION OF MYRCENE WITH METHYL ACRYLATE AT COMPLEX COBALT CATALYSTS

Zakharkin, L. I.,Petrushkina, E. A.

, p. 441 - 443 (2007/10/02)

During the codimerization of myrcene with methyl acrylate at complex cobalt catalysts a mixture of four linear codimers is formed, i.e., methyl 5-ethylidene-9-methyl-(E)-2,8- and 5-ethylidene-9-methyl-(Z)-2,8-decadienoates and methyl 6,10-dimethyl-(E)-2,5,9- and 6,10-dimethyl-(Z)-2,5,9-undecatrienoates.

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