기본 정보
- 표준 SMILES
[Cl-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1- InChIKey
ZFEAYIKULRXTAR-UHFFFAOYSA-M- 분자식
- C18H15S.Cl
- 평균 분자량
- 298.8 g/mol
- 단동위원소 질량
- 298.05829916
개요
RN given refers to chloride
이름 및 식별자
- 우선 이름
- Triphenylsulfonium chloride
- IUPAC
- triphenylsulfanium chloride
- 영어명
- Triphenylsulfonium chloride
- 분자식
- C18H15ClS
- 분자량
- 298.83
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
4270-70-6- PubChem CID
- 61343
- DTXSID
DTXSID5052096- UNII
- 93VMP8WB2Z
- EC Number
- 224-259-6
물성
구조 계산 물성
- 극성 표면적
- 1 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 1
- 회전 가능 결합 수
- 3
- 무거운 원자 수
- 20
- 형식 전하
- 0
- 복잡도
- 202
물리화학적 성질
- 녹는점
- 277 °C · 277 °C
- 저장 조건
- 2 · under inert gas (nitrogen or Argon) at 2-8°C
- 물리적 상태
- 가루
- 색상
- 희미한 노란색
- 수용성
- 물에 용해됩니다.
- InChI
- InChI=1S/C18H15S.ClH/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;/h1-15H;1H/q+1;/p-1
- InChIKey
- ZFEAYIKULRXTAR-UHFFFAOYSA-M
- SMILES
- [S+](C1=CC=CC=C1)(C1=CC=CC=C1)C1C=CC=CC=1.[Cl-]
- EPA
- Triphenylsulfonium chloride (4270-70-6)
안전 및 규제
GHS 분류
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 46 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
Regulatory Information
Chemical: Sulfonium, triphenyl-, chloride
Sulfonium, triphenyl-, chloride: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
안전 데이터
- wgk
- 3
- HS 번호
- 2930909899
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 26
화학 및 산업
응용 분야
용도Triphenylsulfonium chloride is used as a key intermediate that is widely used in the new electronic chemicals such as semiconductor, LCD and TFT. It is also used as a photoacid generator (PAG) in Catalyst activation through in situ photogeneration of ligands.
제조 방법
Triphenylsulfonium Chloride Synthesis: Diphenyl sulfoxide, 40 g (0.2 mole), was dissolved in 400 g of dichloroethane, which was stirred under ice cooling. At a temperature below 20° C., 65 g (0.6 mole) of trimethylsilyl chloride was added dropwise to the solution, which was aged for 30 minutes at the temperature. Then, a Grignard reagent which had been prepared from 14.6 g (0.6 mole) of metallic magnesium, 67.5 g (0.6 mole) of chlorobenzene and 168 g of tetrahydrofuran (THF) was added dropwise at a temperature below 20° C. The reaction solution was aged for one hour, after which 50 g of water at a temperature below 20° C. was added to quench the reaction. To this solution, 150 g of water, 10 g of 12N hydrochloric acid, and 200 g of diethyl ether were further added.The water layer was separated and washed with 100 g of diethyl ether, yielding an aqueous solution of triphenylsulfonium chloride. The compound in aqueous solution form was used in the subsequent reaction without further isolation.
상·하류 제품 정보
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