基本情報
- CAS
1719-58-0- 標準SMILES
C=C[Si](C)(C)Cl- InChIKey
XSDCTSITJJJDPY-UHFFFAOYSA-N- 分子式
- C4H9ClSi
- 平均分子量
- 120.65 g/mol
- 単同位体質量
- 120.0162045
名称と識別子
- 優先名称
- Chloro(dimethyl)vinylsilane
- IUPAC
- chloro-ethenyl-dimethylsilane
- 現地名
- クロロジメチルビニルシラン
- 英語名
- Chlorodimethylvinylsilane
- 分子式
- C4H9ClSi
- 分子量
- 120.65
名称と別名
名称をさらに表示
データベース識別子
- CAS
1719-58-0- PubChem CID
- 519368
- DTXSID
DTXSID5042378- ChEMBL
CHEMBL3561435- UNII
- XJA6N5221T
- EC Number
- 217-007-1
- Nikkaji
- J203.112D
物性
構造計算による物性
- 極性表面積
- 0 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 0
- 回転可能結合数
- 1
- 重原子数
- 6
- 形式電荷
- 0
- 複雑度
- 58.6
実験および物理化学的性質
Physical Description
Liquid
Colorless or brown liquid; [Alfa Aesar MSDS]
物理化学的性質
- 沸点
- 82 · 82-83 °C(lit.)
- 比重(密度)
- 0.874 g/mL · 0.874 g/mL at 25 °C(lit.)
- 蒸気圧
- 95 hPa · 95hPa at 20℃
- 屈折率
- 20 · n20/D 1.414(lit.)
- 闪点
- 23 °F · 23 °F
- 貯蔵温度
- 2 · Inert atmosphere,2-8°C
- 溶解性
- 2 Cl2 · ほとんどの非プロトン性有機溶媒、最も一般的には CH2Cl2 に可溶で、H2O や他のプロトン性溶媒と反応します。
- 外見
- clear liquid
- 色
- Colorless to Light yellow to Light orange
- 比重
- 0.884 · 0.884
- 水溶解度
- 水と反応する。
- BRN
- 1737688 · 1737688
- InChI
- 1S/C4H9ClSi/c1-4-6(2,3)5/h4H,1H2,2-3H3
- InChIKey
- XSDCTSITJJJDPY-UHFFFAOYSA-N
- SMILES
- C[Si](C)(Cl)C=C
- CAS データベース
- 1719 · 1719-58-0(CAS DataBase Reference)
- NISTの化学物質情報
- Vinyldimethylchlorosilane(1719-58-0)
- EPAの化学物質情報
- Silane, chloroethenyldimethyl- (1719-58-0)
化学的性質
化学的特性clear light beige to amber liquid
安全と法規制
GHS分類
GHS Classification
Danger
H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P260, P264, P264+P265, P270, P280, P301+P317, P301+P330+P331, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P321, P330, P363, P370+P378, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 132 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
Regulatory Information
Chemical: Silane, chloroethenyldimethyl-
Silane, chloroethenyldimethyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Silane, chloroethenyldimethyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 16-05-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/16026
Silane, chloroethenyldimethyl-: 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.
安全と保護具
Exposure Control and Personal Protection
TIH (Toxic Inhalation Hazard) - Term used to describe gases and volatile liquids that are toxic when inhaled. Some are TIH materials themselves, e.g., chlorine, and some release TIH gases when spilled in water, e.g., chlorosilanes. [ERG 2016].
毒性情報
安全データ
- F
- 1-10
- wgk
- 1
- tsca
- TSCA listed
- ridadr
- UN 2985 3/PG 2
- hs_code
- 29319090
- risk_code
- 11-14-34
- 化審法
- (2)-2042
- 消防法
- 危-4-1-II
- hazard_code
- F,C
- safety_code
- 16-26-33-36/37/39-45-25
- hazard_class
- 3
- packing_group
- II
- Hazard Classifications
- Flam. Liq. 2Skin Corr. 1B
- ストレージクラス
- 3 - Flammable liquids
化学と産業
用途と製造
General Manufacturing Information
All Other Basic Inorganic Chemical Manufacturing
Silane, chloroethenyldimethyl-: ACTIVE
応用分野
使用Metallacycloalkanones have been prepared by the cyclic hydroboration of dialkenyl silanes. In order to obtain one such dialkenyl silane, chlorodimethylvinylsilane was allylated with allyl magnesium bromide (eq 4).The dialkenyl silane was then hydroborated sequentially with thexylborane, followed by treatment with potassium cyanide, trifluoroacetic anhydride, and finally hydrogen peroxide in sodium hydroxide to produce the silacycloheptanone (eq 4).Cyclic silylketones were then further reacted to form acyclic compounds with chiral centers that are difficult to introduce without the use of the silicon tether.
一般的な説明Chloro(dimethyl)vinylsilane (Dimethylvinylchlorosilane, Vinyldimethylchlorosilane, C4H9ClSi) is an organosilicon compound. It participates in the preparation of 1,1,2,2-tetramethyl-1,2-divinyldisilane. It undergoes [2+4] cycloaddition reaction with t-butyllithium in the presence of 2,3-dimethyl-1,3-butadiene to afford cycloadducts.
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