기본 정보
- 표준 SMILES
CCOC(=O)C[Si](C)(C)C- InChIKey
QQFBQBDINHJDMN-UHFFFAOYSA-N- 분자식
- C7H16O2Si
- 평균 분자량
- 160.29 g/mol
- 단동위원소 질량
- 160.09195628
이름 및 식별자
- 우선 이름
- Ethyl trimethylsilylacetate
- IUPAC
- ethyl 2-trimethylsilylacetate
- 영어명
- Ethyl (trimethylsilyl)acetate
- 분자식
- C7H16O2Si
- 분자량
- 160.29
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
4071-88-9- PubChem CID
- 77687
- DTXSID
DTXSID10193694- UNII
- JJ5WZD3DYT
- EC Number
- 223-783-2
- Nikkaji
- J217.879F
물성
구조 계산 물성
- 극성 표면적
- 26.3 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 4
- 무거운 원자 수
- 10
- 형식 전하
- 0
- 복잡도
- 115
실험 및 물리화학적 성질
물리화학적 성질
- 끓는 점
- 156 · 156-159 °C (lit.)
- 밀도
- 0.876 g/mL · 0.876 g/mL at 25 °C (lit.)
- 굴절률
- 20 · n20/D 1.415(lit.)
- 인화점
- 95 °F · 95 °F
- 저장 조건
- Inert atmosphere,Room Temperature
- 용해도
- sol ethereal and chlorinated solvents; reacts with protic solvents.
- 물리적 상태
- 투명한 액체
- 색상
- 무색 내지 거의 무색
- Specific Gravity
- 0.876 · 0.876
- 수용성
- 분해
- BRN
- 1755902 · 1755902
- InChI
- 1S/C7H16O2Si/c1-5-9-7(8)6-10(2,3)4/h5-6H2,1-4H3
- InChIKey
- QQFBQBDINHJDMN-UHFFFAOYSA-N
- SMILES
- CCOC(=O)C[Si](C)(C)C
- NIST
- Ethyl (trimethylsilyl)acetate(4071-88-9)
화학적 성질
Ethyl trimethylsilylacetate is a clear colorless liquid. It is stable to the usual manipulations, and can be stored in glass containers for years without change of physical and spectral properties.
안전 및 규제
GHS 분류
GHS Classification
Warning
H226 (97.8%): Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 45 reports by companies from 4 notifications to the ECHA C&L Inventory.
유해성 정보
안전 데이터
- wgk
- 3
- tsca
- Yes
- ridadr
- UN 3272 3/PG 3
- HS 번호
- 29319090
- risk_code
- 10
- safety_code
- 16-24/25
- 포장분류
- III
- 위험 등급
- 3
- F 고인화성물질
- 10-21
- Hazard Classifications
- Flam. Liq. 2
- 스토리지 클래스
- 3 - Flammable liquids
화학 및 산업
응용 분야
용도Ethyl trimethylsilylacetate is used in the synthesis of ethyl-2,2-dibromo-2-(trimethylsilyl)acetate and α,β-unsaturated esters. It was also used to silylate the enolizable aldehydes and ketones.
일반 설명Reaction of ethyl trimethylsilylacetate (ETSA) with dilute hydrochloric acid, dilute alkali, anhydrous HCl, anhydrous bromine and absolute ethanol has been reported. ETSA undergoes condensation with aromatic aldehydes in the presence of base catalyst to yield β-trimethylsiloxycarboxylates. Lithium ETSA reacts with ketones to yield α,β-unsaturated esters.
제조 방법
ethyl trimethylsilylacetate synthesis: Available by a Reformatsky reaction from ethyl bromoacetate, and by reaction of trimethylsilylmethylmagnesium chloride with ethyl chloroformate. An alternative approach requires the treatment of ethyl acetate with triphenylmethylsodium followed by chlorotrimethylsilane The use of a nitrogen base with ethyl acetate in THF followed by reaction with chlorotrimethylsilane results in a mixture of C- and O-silylation. The use of HMPA as additive in the reaction medium increases the amount of O-silylation to 90%. Similar methods can be used to prepare analogs.
상·하류 제품 정보
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하류 제품
공급사50 곳
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