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121601-93-2

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121601-93-2 Usage

General Description

1-Adamantylacrylate is a chemical compound that is primarily used as a monomer in the production of polymers and plastics. It is a clear, colorless liquid with a high boiling point and low volatility, making it suitable for use in a wide range of industrial applications. This chemical is known for its high thermal stability, excellent adhesion properties, and resistance to abrasion and chemicals, making it an important ingredient in the manufacturing of adhesives, coatings, and resins. Additionally, 1-Adamantylacrylate is used in the production of specialty polymers for optical and electronic materials due to its exceptional optical transparency and electrical properties. It is essential in various high-performance materials and is valued for its unique combination of mechanical, thermal, and electrical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 121601-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,0 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121601-93:
(8*1)+(7*2)+(6*1)+(5*6)+(4*0)+(3*1)+(2*9)+(1*3)=82
82 % 10 = 2
So 121601-93-2 is a valid CAS Registry Number.

121601-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Adamantan-1-yl acrylate

1.2 Other means of identification

Product number -
Other names 1-adamantyl prop-2-enoate

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:121601-93-2 SDS

121601-93-2Relevant articles and documents

Synthesis and thermal, optical, and mechanical properties of sequence-controlled poly(1-adamantyl acrylate)-block-poly(n-butyl acrylate) containing polar side group

Nakano, Yoshinori,Sato, Eriko,Matsumoto, Akikazu

, p. 2899 - 2910 (2014)

We prepared the sequence-controlled block copolymers including poly(1-adamantyl acrylate) (PAdA) and poly(n-butyl acrylate) sequences as the hard and soft segments, respectively, by the organotellurium-mediated living radical polymerization. The thermal,

Synthesis of organic-inorganic polymer hybrids by means of host-guest interaction utilizing cyclodextrin

Ogoshi, Tomoki,Chujo, Yoshiki

, p. 654 - 660 (2003)

Organic -inorganic polymer hybrids were synthesized utilizing the host-guest interaction. Cyclodextrins (CDs, α-, β-, γ-CD) could be dispersed in the silica gel matrix at a nanometer level because of the hydrogen-bonding interaction between hydroxyl moieties of CD and residual silanol groups of silica gel. It is known that β-CD forms a strong host-guest complex with l-adamantanol in an aqueous solution. Thus, the organic polymer modified with an adamantane group at the side chain (ADA-PAA) and silica gel hybrids could be prepared by complexation of β-CD with ADA-PAA. β-CD played a role as a compatibilizer between ADA-PAA and silica gel to obtain transparent and homogeneous polymer hybrids. The evidence of the host-guest complex formation was confirmed by a fluorescence technique using a dansyl group. Furthermore, transparent and homogeneous CD-polymer complex/silica gel hybrids were prepared utilizing CDs formed polyrotaxane-type inclusion complexes with polymers, such as poly(ethylene glycol) and polyisobutylene.

Activated Self-Resolution and Error-Correction in Catalytic Reaction Networks**

Schaufelberger, Fredrik,Ramstr?m, Olof

supporting information, p. 10335 - 10340 (2021/05/07)

Understanding the emergence of function in complex reaction networks is a primary goal of systems chemistry and origin-of-life studies. Especially challenging is to create systems that simultaneously exhibit several emergent functions that can be independently tuned. In this work, a multifunctional complex reaction network of nucleophilic small molecule catalysts for the Morita-Baylis-Hillman (MBH) reaction is demonstrated. The dynamic system exhibited triggered self-resolution, preferentially amplifying a specific catalyst/product set out of a many potential alternatives. By utilizing selective reversibility of the products of the reaction set, systemic thermodynamically driven error-correction could also be introduced. To achieve this, a dynamic covalent MBH reaction based on adducts with internal H-transfer capabilities was developed. By careful tuning of the substituents, rate accelerations of retro-MBH reactions of up to four orders of magnitude could be obtained. This study thus demonstrates how efficient self-sorting of catalytic systems can be achieved through an interplay of several complex emergent functionalities.

Phosphine-Catalyzed Cascade Annulation of MBH Carbonates and Diazenes: Synthesis of Hexahydrocyclopenta[c]pyrazole Derivatives

Guo, Hongchao,Li, Hongxiang,Liu, Hao,Shi, Wangyu,Wang, Chang,Wang, Wei,Wu, Yongjun

supporting information, p. 5571 - 5575 (2021/07/31)

A phosphine-catalyzed cascade annulation of Morita-Baylis-Hillman (MBH) carbonates and diazenes was achieved, giving tetrahydropyrazole-fused heterocycles bearing two five-membered rings in moderate to excellent yields. The reaction underwent an unprecedented reaction mode of MBH carbonates, in which two molecules of MBH carbonates were fully merged into the ring system.

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