기본 정보
- 표준 SMILES
CC[Si](CC)(CC)OS(=O)(=O)C(F)(F)F- InChIKey
STMPXDBGVJZCEX-UHFFFAOYSA-N- 분자식
- C7H15F3O3SSi
- 평균 분자량
- 264.34 g/mol
- 단동위원소 질량
- 264.04632653
이름 및 식별자
- 우선 이름
- Triethylsilyl trifluoromethanesulphonate
- IUPAC
- triethylsilyl trifluoromethanesulfonate
- 영어명
- Triethylsilyl trifluoromethanesulfonate
- 분자식
- C7H15F3O3SSi
- 분자량
- 264.34
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
79271-56-0- PubChem CID
- 2733308
- DTXSID
DTXSID00229597- EC Number
- 279-124-4
- Nikkaji
- J267.450E
물성
구조 계산 물성
- 극성 표면적
- 51.8 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 6
- 회전 가능 결합 수
- 5
- 무거운 원자 수
- 15
- 형식 전하
- 0
- 복잡도
- 281
물리화학적 성질
- 끓는 점
- 85 · 85-86 °C/12 mmHg (lit.)
- 밀도
- 1.169 g/mL · 1.169 g/mL at 25 °C (lit.)
- 굴절률
- 20 · n20/D 1.389(lit.)
- 인화점
- 162 °F · 162 °F
- 저장 조건
- Inert atmosphere,Room Temperature
- 용해도
- 2 Cl2 · Triethylsilyl Trifluoromethanesulfonate is readily sol hydrocarbons, dialkyl ethers, halogenated solvents. CH2Cl2 is employed most commonly. Reactions in 1,2-dichloroethane proceed faster than those in CCl4 or Et2O. Protic solvents and THF react with trialkylsilyl triflates and are therefore not suitable.
- 물리적 상태
- 발연 액체
- Specific Gravity
- 1.169 · 1.169
- 색상
- 투명한 무색~연한 갈색
- 수용성
- 디클로로메탄, 탄화수소, 디알킬 에테르 및 할로겐화 용매와 혼합 가능합니다. 물과 섞이지 않습니다.
- BRN
- 3590541 · 3590541
- 안정성
- Moisture Sensitive and Hygroscopic, Moisture Sensitive And Hygroscopic
- InChI
- 1S/C7H15F3O3SSi/c1-4-15(5-2,6-3)13-14(11,12)7(8,9)10/h4-6H2,1-3H3
- InChIKey
- STMPXDBGVJZCEX-UHFFFAOYSA-N
- SMILES
- CC[Si](CC)(CC)OS(=O)(=O)C(F)(F)F
화학적 성질
clear colorless to light brown fuming liquid
안전 및 규제
GHS 분류
GHS Classification
Danger
H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 47 reports by companies from 4 notifications to the ECHA C&L Inventory.
유해성 정보
안전 데이터
- wgk
- 3
- tsca
- No
- ridadr
- UN 3265 8/PG 2
- HS 번호
- 29319090
- risk_code
- 34-14
- hazard_code
- C,F
- safety_code
- 26-36/37/39-45-27
- 포장분류
- II
- 위험 등급
- 8
- F 고인화성물질
- 10-21
- 위험 참고 사항
- Corrosive/Flammable
- Hazard Classifications
- Skin Corr. 1B
- 스토리지 클래스
- 8A - Combustible corrosive hazardous materials
화학 및 산업
응용 분야
용도Triethylsilyl Trifluoromethanesulfonate can be used as potent silylating agent and as Lewis acid catalyst. Triethylsilyl ethers are generally more stable towards hydrolysis than are trimethylsilyl ethers, and consequently the Et3Si moiety has gained increasing use as a protecting group for alcohols. However, since it is often difficult to silylate sterically hindered hydroxyl groups using Et3SiCl, triethylsilyl perchlorate and triethylsilyl triflate (Et3SiOTf) were introduced to overcome this problem. Jefford has reported that condensation reactions of 2-trimethylsiloxyfuran with aldehydes can be catalyzed by Et3SiOTf to give mainly the threo addition product (eq 8).
제조 방법
Triethylsilyl Trifluoromethanesulfonate can be prepared by reacting chlorotriethylsilane with trifluoromethanesulfonic acid followed by distillation.
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