2-메틸-2-Adamantyl 메타아크릴레이트

2-메틸-2-Adamantyl 메타아크릴레이트
2-메틸-2-Adamantyl 메타아크릴레이트 구조식 이미지
카스 번호:
177080-67-0
한글명:
2-메틸-2-Adamantyl 메타아크릴레이트
동의어(한글):
2-메틸-2-Adamantyl메타아크릴레이트;2-메틸-2-아다아만틸메타아크릴레이트;2-메틸-2-아다만틸메타크릴레이트
상품명:
2-Methacryloyloxy-2-methyladamantane
동의어(영문):
2-METHYL-2-ADAMANTYL METHACRYL;-Methyl-2-adamantylmethacrylate;2-Ethy1-2-adamantylmethacrylate;2-Methyl-2-adaMantyl Methacrylte;2-Methyl-2-adamantyl methacrylate;2-MethyladaMantan-2-yl Methacrylate;2-methacryloyloxy-2-methyladamantane;2-Methyl-2-adamantyl methacrylate (MADMA);Methacrylic Acid 2-Methyl-2-adamantyl Ester;2-Methyl-2-adamantylmethacrylate 177080-67-0
CBNumber:
CB31483683
분자식:
C15H22O2
포뮬러 무게:
234.33
MOL 파일:
177080-67-0.mol

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
기존화학 물질 2001-3-1920
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
예방조치문구:
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
1
0 0

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%.

177080-67-0.png

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

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