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444315-18-8

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  • 1-VINYL-3,5,7,9,11,13,-ISOBUTYLPENTACYCL0-(9.5.1.1(3,9).1(5,15).1(7)OCTASILOXANE

    Cas No: 444315-18-8

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444315-18-8 Usage

General Description

PSS-VINYL-HEPTAISOBUTYL SUBSTITUTED is a chemical compound that belongs to the vinyl polymer group. It is characterized by the presence of heptaisobutyl substituents, which are long-chain hydrocarbon groups that provide the molecule with unique properties. This chemical is commonly used in coatings, adhesives, and sealants, where its long-chain structure and vinyl functionality contribute to enhanced adhesion and durability. It is also known for its high chemical resistance and flexibility, making it a preferred choice for applications that require a strong and reliable protective layer. Additionally, PSS-VINYL-HEPTAISOBUTYL SUBSTITUTED has potential applications in the pharmaceutical and biomedical industries due to its biocompatibility and low toxicity. Overall, this compound is a versatile and valuable material with a wide range of industrial and commercial uses.

Check Digit Verification of cas no

The CAS Registry Mumber 444315-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,3,1 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 444315-18:
(8*4)+(7*4)+(6*4)+(5*3)+(4*1)+(3*5)+(2*1)+(1*8)=128
128 % 10 = 8
So 444315-18-8 is a valid CAS Registry Number.

444315-18-8 Well-known Company Product Price

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  • Aldrich

  • (560367)  PSS-Vinyl-Heptaisobutylsubstituted  

  • 444315-18-8

  • 560367-1G

  • 603.72CNY

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  • Aldrich

  • (560367)  PSS-Vinyl-Heptaisobutylsubstituted  

  • 444315-18-8

  • 560367-5G

  • 2,075.58CNY

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444315-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name MonovinylIsobutyl-POSS?

1.2 Other means of identification

Product number -
Other names vinylheptaisobutyl-T8-silsesquioxane

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:444315-18-8 SDS

444315-18-8Relevant articles and documents

Sequence-Mandated, Distinct Assembly of Giant Molecules

Zhang, Wei,Lu, Xinlin,Mao, Jialin,Hsu, Chih-Hao,Mu, Gaoyan,Huang, Mingjun,Guo, Qingyun,Liu, Hao,Wesdemiotis, Chrys,Li, Tao,Zhang, Wen-Bin,Li, Yiwen,Cheng, Stephen Z. D.

, p. 15014 - 15019 (2017)

Although controlling the primary structure of synthetic polymers is itself a great challenge, the potential of sequence control for tailoring hierarchical structures remains to be exploited, especially in the creation of new and unconventional phases. A series of model amphiphilic chain-like giant molecules was designed and synthesized by interconnecting both hydrophobic and hydrophilic molecular nanoparticles in precisely defined sequence and composition to investigate their sequence-dependent phase structures. Not only compositional variation changed the self-assembled supramolecular phases, but also specific sequences induce unconventional phase formation, including Frank–Kasper phases. The formation mechanism was attributed to the conformational change driven by the collective hydrogen bonding and the sequence-mandated topology of the molecules. These results show that sequence control in synthetic polymers can have a dramatic impact on polymer properties and self-assembly.

Efficient functionalisation of cubic monovinylsilsesquioxanes via cross-metathesis and silylative coupling with olefins in the presence of ruthenium complexes

Zak, Patrycja,Pietraszuk, Cezary,Marciniec, Bogdan,Spolnik, Brzegorz,Danikiewicz, Witold

experimental part, p. 2675 - 2682 (2010/04/05)

Monovinylheptaisobutylsilsesquioxane undergoes efficient cross-metathesis and silylative coupling with styrenes. Allyl derivatives were successfully tested in cross-metathesis in the presence of first generation Grubbs' catalyst, while heteroatom-substitu

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