2-메틸-2-Adamantyl 메타아크릴레이트
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2-메틸-2-Adamantyl 메타아크릴레이트 속성
- 끓는 점
- 301.3±11.0 °C(Predicted)
- 밀도
- 1.06±0.1 g/cm3(Predicted)
- 굴절률
- 1.5050 to 1.5090
- 인화점
- 120°C(lit.)
- 저장 조건
- 2-8°C
- 물리적 상태
- 투명한 액체
- 색상
- 무색 내지 거의 무색
- Specific Gravity
- 1.06
- 감도
- Heat Sensitive
- InChI
- InChI=1S/C15H22O2/c1-9(2)14(16)17-15(3)12-5-10-4-11(7-12)8-13(15)6-10/h10-13H,1,4-8H2,2-3H3
- InChIKey
- FDYDISGSYGFRJM-UHFFFAOYSA-N
- SMILES
- C(OC1(C)C2CC3CC1CC(C3)C2)(=O)C(C)=C
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
HS 번호 | 2902190000 | ||
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기존화학 물질 | 2001-3-1920 |
2-메틸-2-Adamantyl 메타아크릴레이트 C화학적 특성, 용도, 생산
화학적 성질
Off-white powder.주요 응용
2-Methacryloyloxy-2-methyladamantane as a guest molecule can be introduced onto the silicon substrate by interacting with β-cyclodextrin (β-CD) to construct supramolecular composite surfaces. After the assembly of hydrophilic guest molecules on the main surface, the wettability, water lubrication and resistance to algal cell adhesion of the supramolecular composite surface were improved. This host-guest interface supramolecule provides a new way to prepare water-based lubrication and antifouling materials[2].Synthesis
The synthesis of 2-Methyl-2-adamantylmethacrylate is as follows:Add 3546ml of n-heptane in the 5L four-necked flask equipped with stirring paddle, condenser tube and thermometer, turn on stirring, add 126.3g of 2-methyladamantanol to the system, and slowly add 0.022g polymerization inhibitor tetrachlorobenzoquinone to the reaction, add 110.8g basic ion exchange resin, adjust pH=7-8, cool down to -13°C, slowly add 110.8g vinyl methacrylate dropwise to the reaction system, keep the reaction for 7h, monitor the reaction progress, and take samples for detection After the reaction was completed, 1000 ml of water was added to the reaction system, and the mixture was stirred and extracted for phase separation. The organic phase was dried, concentrated under reduced pressure and evaporated to dryness to obtain 167 g of 2-methyl-2-adamantyl methacrylate (2-Methacryloyloxy-2-methyladamantane) product with a yield of 93.78%.
참고 문헌
[1] M. Maríc. “Nitroxide‐mediated polymerization of adamantyl‐functional methacrylates for 193 nm photoresists.” Canadian Journal of Chemical Engineering 95 1 (2017): 708–716.[2] RONGNIAN XU. Promoting Lubricity and Antifouling Properties by Supramolecular-Recognition-Based Surface Grafting[J]. Langmuir, 2018. DOI:10.1021/acs.langmuir.8b02375.
2-메틸-2-Adamantyl 메타아크릴레이트 준비 용품 및 원자재
원자재
준비 용품
2-메틸-2-Adamantyl 메타아크릴레이트 공급 업체
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Changzhou waston chemical technology Co.,Ltd | +86-051985861892 +8618112881323 |
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Shanghai Z&T Chemical Co., Ltd | +86-021-33561011 +8613818804961 |
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Shanghai Daken Advanced Materials Co.,Ltd | +86-371-66670886 |
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career henan chemical co | +86-0371-86658258 +8613203830695 |
sales@coreychem.com | China | 29888 | 58 |
Shanghai Arbor Chemical Co., Ltd. | 021-60451682 |
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Biochempartner | 0086-13720134139 |
candy@biochempartner.com | CHINA | 967 | 58 |
QINGDAO HONG JIN CHEMCIAL CO.,LTD. | 532-83657313 |
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Shenzhen Nexconn Pharmatechs Ltd | +86-755-89396905 +86-15013857715 |
admin@nexconn.com | China | 10311 | 58 |