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5-(1,3-Dimethylbutylidene)-1,3-cyclopentadiene is an organic compound with the molecular formula C11H16. It is a conjugated diene, featuring a cyclopentadiene ring with a 1,3-dimethylbutylidene group attached at the 5-position. 5-(1,3-Dimethylbutylidene)-1,3-cyclopentadiene is known for its unique chemical structure, which allows it to participate in various chemical reactions, such as Diels-Alder reactions, due to the presence of the reactive diene system. It is often used as an intermediate in the synthesis of more complex organic molecules and has potential applications in the pharmaceutical and chemical industries. The compound's properties, such as its reactivity and stability, make it a valuable building block in organic synthesis.

7338-49-0

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7338-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7338-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7338-49:
(6*7)+(5*3)+(4*3)+(3*8)+(2*4)+(1*9)=110
110 % 10 = 0
So 7338-49-0 is a valid CAS Registry Number.

7338-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methylpentan-2-ylidene)cyclopenta-1,3-diene

1.2 Other means of identification

Product number -
Other names 5-(1,3-Dimethylbutylidene)-1,3-cyclopentadiene

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:7338-49-0 SDS

7338-49-0Downstream Products

7338-49-0Relevant academic research and scientific papers

Alkenylsubstituierte Calcocene

Westerhausen, Matthias,Hartmann, Manfred,Schwartz, Wolfgang

, p. 359 - 368 (1995)

The reaction of calcium bis with 6-methyl-6-organylfulvene yields calcium bis(1-organyl-ethen-1-yl-cyclopentadienide) with organyl groups such as methyl (1), phenyl (2) and iso-butyl (3).Compound 2 crystallizes in the monoclinic s

Synthesis and characterization of alkenyl and alkyl substituted group 4 metallocene dichloride complexes: Applications in ethylene polymerization

Ceballos-Torres, Jesús,Gómez-Ruiz, Santiago,Fajardo, Mariano,Pinar, Ana B.,Prashar, Sanjiv

, (2019)

The alkenyl substituted zirconocene complexes, [Zr(η5-C5H4{CMeRCH2CH2CH = CMe2})2Cl2] (R = Me (1), Ph (2) were prepared from the reaction of the lithium derivative Li(C5H4{CMeRCH2CH2CH = CMe2}) (R = Me, Ph) with zirconium tetrachloride. The bulky alkyl substituted cyclopentadienyl ligand precursor was prepared as its fulvene derivative (C5H4) = CMeCH2CHMe2 (3) via the reaction of cyclopentadiene with 4-methyl-2-pentanone and then converted to Li(C5H4{CMe2CH2CHMe2}) (4) via nucleophilic attack of LiMe. The reaction of 4 with [TiCl4(THF)2] and ZrCl4 gave the metallocene complexes [M(η5-C5H4{CMe2CH2CHMe2})2Cl2] (M = Ti (5), Zr (6)), respectively. The ansa-ligand precursor, SiMe2(C5HMe4)(C5H4{CMe2CH2CHMe2}) (7), was prepared via the reaction of 4 with SiMe2(C5HMe4)Cl and subsequently converted to its dilithium derivate, Li2(Me2Si(C5Me4)(C5H3{CMe2CH2CHMe2})) (8), using n-butyllithium. The ansa-zirconocene complex, [Zr{Me2Si(η5-C5Me4)(η5-C5H3{CMe2CH2CHMe2})}Cl2] (9), was synthesized by the reaction of 8 with zirconium tetrachloride. Compounds 1–9 were characterized by 1H and 13C{1H} NMR spectroscopy. In addition, the molecular structures of 5, 6 and 9 were determined by single crystal X-ray diffraction studies. The metallocene complexes have been tested as catalyst (with co-catalyst MAO) in the polymerization of ethylene where the substituents on the cyclopentadienyl ligand have a direct influence on the catalytic activity.

METALLOCENE COMPOUND, PROCESS FOR PRODUCING METALLOCENE COMPOUND, OLEFIN POLYMERIZATION CATALYST, PROCESS FOR PRODUCING POLYOLEFIN, AND POLYOLEFIN

-

, (2008/06/13)

The metallocene compound according to the invention and the olefin polymerization catalyst containing the compound are intended to produce a catalyst capable of preparing an isotactic polymer with a high polymerization activity. The metallocene compound contains a substituted cyclopentadienyl group and a (substituted) fluorenyl group and has a structure wherein these groups are bridged by a hydrocarbon group or the like. The process for preparing a metallocene compound according to the invention is intended to selectively prepare a specific metallocene compound so as not to produce an isomer, and in this process an intermediate product is synthesized by a specific method. The process for preparing a polyolefin according to the invention is intended to prepare a polyolefin having excellent impact resistance and transparency, and this process comprises homopolymerizing an α-olefin of 3 to 8 carbon atoms or copolymerizing an olefin of 3 to 8 carbon atoms and another α-olefin in the presence of an olefin polymerization catalyst containing the above-mentioned metallocene compound.

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