기본 정보
- CAS
71550-63-5- 표준 SMILES
C=CC(=O)OCCC[Si](C)(Cl)Cl- InChIKey
GBAQKTTVWCCNHH-UHFFFAOYSA-N- 분자식
- C7H12Cl2O2Si
- 평균 분자량
- 227.16 g/mol
- 단동위원소 질량
- 225.99836151
이름 및 식별자
- 우선 이름
- 3-(Dichloromethylsilyl)propyl 2-propenoate
- IUPAC
- 3-[dichloro(methyl)silyl]propyl prop-2-enoate
- 영어명
- (3-Acryloxypropyl)methyldichlorosilane
- 분자식
- C7H12Cl2O2Si
- 분자량
- 227.16
이름 및 동의어
71550-63-53-(Dichloromethylsilyl)propyl 2-propenoateRefChem:2753693-[dichloro(methyl)silyl]propyl prop-2-enoate(3-ACRYLOXYPROPYL)METHYLDICHLOROSILANE3-acryloxypropylmethyldichlorosilaneMFCD000548283-(dichloro(methyl)silyl)propyl acrylateC7H12Cl2O2SiSCHEMBL840779AcryloxypropylmethyldichlorosilaneDTXSID20992099
이름 더 보기
DK373(3-acryloxypropyl)Methyldichloresilane3-(dichloromethylsilyl)propyl acrylate3-(methyldichlorosilyl)propyl acrylate[3-(Acryloyloxy)propyl](methyl)dichlorosilanePropenoic acid 3-[dichloro(methyl)silyl]propyl ester2-Propenoic acid, 3-(dichloromethylsilyl)propyl ester
NS00062663S001253-(Dichloromethylsilyl)propyl acrylate, EINECS 275-614-7, CID6337315, (3-(Acryloyloxy)propyl)dichloromethylsilane, Silane, (3-(acryloxy)propyl)dichloromethyl-, 2-Propenoic acid, 3-(dichloromethylsilyl)propyl ester, 71550-63-5
데이터베이스 식별자
- CAS
71550-63-5- PubChem CID
- 9964588
- DTXSID
DTXSID20992099- EC Number
- 275-614-7
- Nikkaji
- J289.210C
물성
구조 계산 물성
- 극성 표면적
- 26.3 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 6
- 무거운 원자 수
- 12
- 형식 전하
- 0
- 복잡도
- 171
물리화학적 성질
- 끓는 점
- 73 °C · 73 °C
- 밀도
- 1.15 · 1.15
- 굴절률
- 1.4585 · 1.4585
- 저장 조건
- 5 ° · below 5° C
- 물리적 상태
- Liquid
- Specific Gravity
- 1.15 · 1.15
- 색상
- Clear to straw.
- 냄새
- Acrid
- InChI
- InChI=1S/C7H12Cl2O2Si/c1-2-6(10)11-4-3-5-12-7(8)9/h2,7H,1,3-5,12H2
- InChIKey
- UYPCIZUYNUWPGX-UHFFFAOYSA-N
- SMILES
- C(OCCC[SiH2]C(Cl)Cl)(=O)C=C
- EPA
- 3 · [3-(Acryloyloxy)propyl]dichloromethylsilane (71550-63-5)
안전 및 규제
안전 데이터
- tsca
- TSCA listed
- ridadr
- 2987
- risk_code
- 34-36/37/38
- safety_code
- 26-36/37/39
화학 및 산업
응용 분야
용도(3-Acryloxypropyl)methyldichlorosilane is an organosilane compound containing a halogen atom (chlorine) and serves as a key raw material for the preparation of cationic etherifying agents. The chlorine atom in this compound undergoes a substitution reaction with the hydroxyl groups in quaternary phosphonium-modified chitosan to yield intermediate 2 and introduce an alkenyl group. Subsequently, using reverse emulsion polymerisation, acrylamide and intermediate 2 undergo a polymerisation reaction to yield quaternary phosphonium polyacrylamide.
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