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61548-33-2

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61548-33-2 Usage

Description

(Isooctadecanoato-O)bis(methacrylato-O)(propan-2-olato)titanium, also known as titanium bis(methacrylato-O)(propan-2-olato), is an organometallic complex with the molecular formula C28H50O8Ti. It features a central titanium atom bonded to two methacrylate groups, an isooctadecanoate group, and a propan-2-olato group. (isooctadecanoato-O)bis(methacrylato-O)(propan-2-olato)titanium is known for its catalytic properties in various polymerization reactions and its utility in the production of acrylic and methacrylic polymers.

Uses

Used in Polymerization Catalysts:
(Isooctadecanoato-O)bis(methacrylato-O)(propan-2-olato)titanium is used as a catalyst or co-catalyst in the polymerization of acrylic and methacrylic monomers. Its application is crucial for the production of high-quality polymers with specific properties tailored for various end-use applications.
Used in Crosslinking Agents:
In the field of materials science, this titanium complex serves as an effective crosslinking agent. It helps in creating a network of chemical bonds between polymer chains, enhancing the mechanical properties, thermal stability, and durability of the final product.
Used in Adhesives and Coatings:
(Isooctadecanoato-O)bis(methacrylato-O)(propan-2-olato)titanium is also utilized as a component in the formulation of adhesives and coatings. Its presence improves the adhesion properties, durability, and resistance to environmental factors such as UV radiation and moisture.
Used in Photovoltaic Devices:
(isooctadecanoato-O)bis(methacrylato-O)(propan-2-olato)titanium has potential applications in the development of photovoltaic devices, where it can contribute to the efficiency and performance of solar panels by enhancing the charge transport and light absorption properties of the materials used.
Used in Electronic Devices:
Beyond photovoltaics, (isooctadecanoato-O)bis(methacrylato-O)(propan-2-olato)titanium may also find use in other electronic devices, where its unique properties can be harnessed to improve the performance of components such as sensors, transistors, and dielectric materials.

Check Digit Verification of cas no

The CAS Registry Mumber 61548-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,4 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61548-33:
(7*6)+(6*1)+(5*5)+(4*4)+(3*8)+(2*3)+(1*3)=122
122 % 10 = 2
So 61548-33-2 is a valid CAS Registry Number.

61548-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 16-methylheptadecanoic acid,2-methylprop-2-enoic acid,propan-2-ol,titanium

1.2 Other means of identification

Product number -
Other names Isopropyl dimethacryl isostearoyl titanate

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:61548-33-2 SDS

61548-33-2Downstream Products

61548-33-2Relevant articles and documents

Heteropoly blue as a reaction-controlled phase-transfer catalyst for the epoxidation of olefins

Mingqiang, Li,Xigao, Jian

, p. 1575 - 1579 (2005)

A new reaction-controlled phase-transfer catalyst system has been designed and synthesized. In this system, heteropoly blue, [C7H 7N(CH3)3]3PMo4O 16, is used for the catalytic epoxidation of olefins with H 2O2 as the oxidant. In this system, the catalyst not only can be recovered, like heterogeneous catalyst, but also acts as a homogeneous catalyst. The main products are epoxide of olefins and H2O; no co-product forms. The system exhibits high conversion and selectivity as well as excellent catalyst stability. 31PNMR spectra, UV-vis spectra, and infrared spectra are used to analyze the reason for the phase transfer of the catalyst, indicating that the change of structure leads to the formation of reaction-controlled phase-transfer catalyst.

Ultraselective epoxidation of butadiene on Cu{111} and the effects of Cs promotion [6]

Cowell, James J.,Santra, Ashok K.,Lambert, Richard M.

, p. 2381 - 2382 (2000)

-

Enantioselective Radical-Polar Crossover Reactions of Indanonecarboxamides with Alkenes

Cao, Weidi,Feng, Xiaoming,Liu, Xiaohua,Wu, Wangbin,Xu, Xi,Yu, Han,Zhang, Xiying

supporting information, p. 4846 - 4850 (2020/02/11)

Highly efficient asymmetric intermolecular radical-polar crossover reactions were realized by combining a chiral N,N′-dioxide/NiII complex catalyst with Ag2O under mild reaction conditions. Various terminal alkenes and indanonecarboxamides/esters underwent radical addition/cyclization reactions to afford spiro-iminolactones and spirolactones with good to excellent yields (up to 99 %) and enantioselectivities (up to 97 % ee). Furthermore, a range of different radical-mediated oxidation/elimination or epoxide ring-opening products were obtained under mild reaction conditions. The Lewis acid catalysts exhibited excellent performance and precluded the strong background reaction.

3,4-epoxy-1-butene preparation method

-

Paragraph 0032-0035, (2017/03/18)

The present invention relates to a 3,4-epoxy-1-butene preparation method. A purpose of the present invention is mainly to solve the problems of low raw material conversion rate, low product yield and serious waste in the prior art. The technical scheme co

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