Grundinformationen
- Standard-SMILES
C=C[Si](C)(C)Cl- InChIKey
XSDCTSITJJJDPY-UHFFFAOYSA-N- Summenformel
- C4H9ClSi
- Durchschnittliche Molmasse
- 120,65 g/mol
- Monoisotopische Masse
- 120,0162045
Namen und Bezeichner
- Bevorzugter Name
- Chloro(dimethyl)vinylsilane
- IUPAC
- chloro-ethenyl-dimethylsilane
- Lokaler Name
- Chlordimethylvinylsilan
- Englischer Name
- Chlorodimethylvinylsilane
- Summenformel
- C4H9ClSi
- Molmasse
- 120.65
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
1719-58-0- PubChem CID
- 519368
- DTXSID
DTXSID5042378- ChEMBL
CHEMBL3561435- UNII
- XJA6N5221T
- EC Number
- 217-007-1
- Nikkaji
- J203.112D
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 0
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 6
- Formalladung
- 0
- Komplexität
- 58,6
Experimentelle und physikochemische Eigenschaften
Physical Description
Liquid
Colorless or brown liquid; [Alfa Aesar MSDS]
Physikochemische Eigenschaften
- Siedepunkt
- 82 · 82-83 °C(lit.)
- Dichte
- 0.874 g/mL · 0.874 g/mL at 25 °C(lit.)
- Dampfdruck
- 95 hPa · 95hPa at 20℃
- Brechungsindex
- 20 · n20/D 1.414(lit.)
- Flammpunkt
- 23 °F · 23 °F
- storage temp.
- 2 · Inert atmosphere,2-8°C
- Löslichkeit
- 2 Cl2 · most aprotic organic solvents, but CH2Cl2 is most commonly used; reacts with H2O and other protic solvents.
- Aggregatzustand
- clear liquid
- Farbe
- Colorless to Light yellow to Light orange
- Wichte
- 0.884 · 0.884
- Wasserlöslichkeit
- Reacts with water.
- 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 Datenbank
- 1719 · 1719-58-0(CAS DataBase Reference)
- NIST chemische Informationen
- Vinyldimethylchlorosilane(1719-58-0)
- EPA chemische Informationen
- Silane, chloroethenyldimethyl- (1719-58-0)
Sicherheit und Regulatorisches
GHS-Klassifizierung
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.
Gefahrenhinweise
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.
Sicherheit und Schutzausrüstung
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].
Toxikologische Informationen
Sicherheitsdaten
- F
- 1-10
- wgk
- 1
- tsca
- TSCA listed
- ridadr
- UN 2985 3/PG 2
- hs_code
- 29319090
- risk_code
- 11-14-34
- hazard_code
- F,C
- safety_code
- 16-26-33-36/37/39-45-25
- hazard_class
- 3
- packing_group
- II
- Speicherklasse
- 3 - Flammable liquids
- Hazard Classifications
- Flam. Liq. 2Skin Corr. 1B
Chemie und Industrie
Verwendung und Herstellung
General Manufacturing Information
All Other Basic Inorganic Chemical Manufacturing
Silane, chloroethenyldimethyl-: ACTIVE
Anwendungen
VerwendenMetallacycloalkanones 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.
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