기본 정보
- 표준 SMILES
C[Si](C)(C)C1SCCCS1- InChIKey
BTTUMVHWIAXYPJ-UHFFFAOYSA-N- 분자식
- C7H16S2Si
- 평균 분자량
- 192.4 g/mol
- 단동위원소 질량
- 192.04626904
이름 및 식별자
- 우선 이름
- 2-Trimethylsilyl-1,3-dithiane
- IUPAC
- 1,3-dithian-2-yl(trimethyl)silane
- 영어명
- 2-TRIMETHYLSILYL-1,3-DITHIANE
- 분자식
- C7H16S2Si
- 분자량
- 192.42
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
13411-42-2- PubChem CID
- 83413
- DTXSID
DTXSID70158542- EC Number
- 236-504-4
- Nikkaji
- J317.864A
물성
구조 계산 물성
- 극성 표면적
- 50.6 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 1
- 무거운 원자 수
- 10
- 형식 전하
- 0
- 복잡도
- 103
실험 및 물리화학적 성질
물리화학적 성질
- 끓는 점
- 54 · 54-55 °C0.17 mm Hg(lit.)
- 밀도
- 1.014 g/mL · 1.014 g/mL at 25 °C(lit.)
- 굴절률
- 20 · n20/D 1.533(lit.)
- 인화점
- 205 °F · 205 °F
- 저장 조건
- 2 · 2-8°C
- 용해도
- 물에 불용성, 유기 용액에 용해됨
- 물리적 상태
- 투명한 액체
- 색상
- Colorless to Light yellow to Light orange
- Specific Gravity
- 1.014 · 1.014
- BRN
- 1616463 · 1616463
- InChI
- 1S/C7H16S2Si/c1-10(2,3)7-8-5-4-6-9-7/h7H,4-6H2,1-3H3
- InChIKey
- BTTUMVHWIAXYPJ-UHFFFAOYSA-N
- SMILES
- C[Si](C)(C)C1SCCCS1
화학적 성질
CLEAR COLORLESS TO SLIGHTLY YELLOW LIQUID
안전 및 규제
GHS 분류
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P273, 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)
The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
유해성 정보
안전 데이터
- wgk
- 3
- tsca
- No
- ridadr
- 3334
- HS 번호
- 2934.99.9001
- safety_code
- 23-24/25
- F 고인화성물질
- 13
- 스토리지 클래스
- 10 - Combustible liquids
화학 및 산업
응용 분야
용도2-Trimethylsilyl-1,3-dithiane is the precursor of dithioketene acetals which are good substrates for both cationic and anionic cyclization processes; the anion reacts with unsaturated ketones and aldehydes to give vinyl dithioketene acetals that can be used as dienes or for the preparation of substituted α,β-unsaturated alkyl ketones; alkylation of the anion provides a general synthesis of acylsilanes. It participates the following reactions: Thioketene Acetals, Cationic and Anionic Cyclizations, Unsaturated Dithioketene Acetals, Acylsilanes, Multicomponent Linchpin Reactions, Formation of Bis(acylsilanes) etc.
일반 설명2-(Trimethylsilyl)-1,3-dithiane participates in Lewis base-catalyzed 1,3-dithiane addition to electrophiles such as carbonyl compounds and N-substituted aldimines. It undergoes novel diazo transfer reaction with tosyl azide in hexamethylphosphoramide-THF to yield 2-diazo-1,3-dithiane, which on decomposition yields formal carbene adducts. It is a versatile acyl anion equivalent.
제조 방법
2-Trimethylsilyl-1,3-dithiane is prepared by alkylation of 2-lithio-1,3- dithiane with chlorotrimethylsilane (eq 1).
상·하류 제품 정보
하류 제품
공급사50 곳
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