Vinyltrimethylsilane
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Vinyltrimethylsilane 속성
- 녹는점
- -132°C
- 끓는 점
- 55 °C (lit.)
- 밀도
- 0.684 g/mL at 25 °C (lit.)
- 증기압
- 4.44 psi ( 20 °C)
- 굴절률
- n
20/D 1.391(lit.)
- 인화점
- <-30 °C
- 저장 조건
- Inert atmosphere,2-8°C
- 용해도
- 테트라히드로푸란, 디에틸 에테르, 벤젠 및 디클로로메탄과 혼합 가능.
- 물리적 상태
- 액체
- Specific Gravity
- 0.6903
- 색상
- 무색 내지 거의 무색
- Hydrolytic Sensitivity
- 1: no significant reaction with aqueous systems
- BRN
- 956572
- InChIKey
- GCSJLQSCSDMKTP-UHFFFAOYSA-N
- CAS 데이터베이스
- 754-05-2(CAS DataBase Reference)
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
위험품 표기 | F,Xn | ||
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위험 카페고리 넘버 | 11-22-36/37/38-40 | ||
안전지침서 | 16-26-33-36-36/37/39-36/37 | ||
유엔번호(UN No.) | UN 1993 3/PG 1 | ||
WGK 독일 | 1 | ||
TSCA | Yes | ||
위험 등급 | 3 | ||
포장분류 | II | ||
HS 번호 | 29319090 |
Vinyltrimethylsilane C화학적 특성, 용도, 생산
화학적 성질
clear colourless liquid물리적 성질
bp 55–57 °C; d20 4 0.691 g cm?3; n20 D 1.391.용도
Vinyltrimethylsilane is ethylene equivalent in electrophilic substitution reactions; precursor to 3-trimethylsilyl-3-buten-2-one, a methyl vinyl ketone surrogate for Robinson annulations; homologation of aldehydes to α,β-unsaturated aldehydes. It takes part in the reactions of Synthesis of Vinyl Aryl Sulfides, Synthesis of 3-Triethylsilyl-3-buten-2-one, Synthesis of α,β-Unsaturated Primary Amides, Synthesis of α,β-Unsaturated Aldehydes, Synthesis of Bicyclopentenones, Synthesis of 1-Chlorocyclopropene, Radical Addition Reactions of Vinyltrimethylsilane, Reaction of Vinyltrimethylsilane with 2-Azaallylanions, Regioselective Hydroesterification of Vinyltrimethylsilane, 3 + 2 Cycloaddition of Vinyltrimethylsilane with Nitrones, Addition of α-Iodo-α,α-Difluoroketones to Vinyltrimethylsilane, Addition of α-Iodosulfones to Vinyltrimethylsilane, Titanium-mediated Formation of Trimethylsilylcyclopropanols, β-Trimethylsilyl Ketones and Cyclopropenes, Hydrogen Acceptor Catalyst in the Conversion of Alcohols to Hydrogenated Wittig Adducts, Formation of 2-Trimethylsilylaziridines, Formation of Sulfonyl Chlorides, Improved Synthesis of 2-Trimethylsilylethylsulfonyl Chloride, Formation of an Iron Carbonyl Trienone Complex, Synthesis of 2-Phenyl-2-Trimethylsilylethanol, Synthesis of 2-Vinylanilines, Decarbonylative Vinylation of an Aromatic Ester, Asymmetric Epoxidation of Vinyltrimethylsilane, Direct Silylation of Heteroarylcarbonyl Compounds, Trimethylsilylation of Vinylboronates, etc.제조 방법
Prepared in 67–91% yield from vinylmagnesium bromide and chlorotrimethylsilane in THF.Purification Methods
If the 1H NMR spectrum shows impurities, then dissolve it in Et2O, wash it with aqueous NH4Cl solution, dry over CaCl2, filter, evaporate and distil it at atmospheric pressure in an inert atmosphere. It is used as a co-polymer and may polymerise in the presence of free radicals. It is soluble in CH2Cl2. [Nagel & Post J Org Chem 17 1379 1952, Beilstein 4 IV 3922.]Vinyltrimethylsilane 준비 용품 및 원자재
원자재
준비 용품
Vinyltrimethylsilane 공급 업체
글로벌( 260)공급 업체
공급자 | 전화 | 이메일 | 국가 | 제품 수 | 이점 |
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Hebei Yanxi Chemical Co., Ltd. | +8617531190177 |
peter@yan-xi.com | China | 5993 | 58 |
Capot Chemical Co.,Ltd. | 571-85586718 +8613336195806 |
sales@capotchem.com | China | 29797 | 60 |
Shanghai Daken Advanced Materials Co.,Ltd | +86-371-66670886 |
info@dakenam.com | China | 15928 | 58 |
Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 |
info@tianfuchem.com | China | 21691 | 55 |
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 |
ivan@atkchemical.com | China | 32480 | 60 |
Kingfirst chemical (nanjing) co.,ltd | 86-25-84522992 |
marketing@kingfirstchem.com | CHINA | 95 | 58 |
Xiamen AmoyChem Co., Ltd | +86-592-6051114 +8618959220845 |
sales@amoychem.com | China | 6387 | 58 |
Chongqing Chemdad Co., Ltd | +86-023-61398051 +8613650506873 |
sales@chemdad.com | China | 39916 | 58 |
career henan chemical co | +86-0371-86658258 15093356674; |
factory@coreychem.com | China | 29826 | 58 |
Hubei Co-Formula Material Tech Co., Ltd. | +86-27-84459282 |
sales@cfmats.com | CHINA | 882 | 58 |