Grundinformationen
- Standard-SMILES
C[Si](Cl)(c1ccccc1)c1ccccc1- InChIKey
OJZNZOXALZKPEA-UHFFFAOYSA-N- Summenformel
- C13H13ClSi
- Durchschnittliche Molmasse
- 232,78 g/mol
- Monoisotopische Masse
- 232,0475046
Namen und Bezeichner
- Bevorzugter Name
- Chloro(methyl)diphenylsilane
- IUPAC
- chloro-methyl-diphenylsilane
- Lokaler Name
- Chlor(methyl)diphenylsilan
- Englischer Name
- Chlorodiphenylmethylsilane
- Summenformel
- C13H13ClSi
- Molmasse
- 232.78
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
144-79-6- PubChem CID
- 67349
- DTXSID
DTXSID3027116- ChEMBL
CHEMBL3182736- EC Number
- 205-639-0
- Nikkaji
- J109.082H
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 0
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 15
- Formalladung
- 0
- Komplexität
- 175
Experimentelle und physikochemische Eigenschaften
Kovats Retention Index
1675.2
1675.5
Physikochemische Eigenschaften
- Schmelzpunkt
- -22 °C · -22°C
- Siedepunkt
- 295 °C · 295 °C (lit.)
- Dichte
- 1.107 g/mL · 1.107 g/mL at 25 °C (lit.)
- Dampfdruck
- 3 mm · 3 mm Hg ( 125 °C)
- Brechungsindex
- 20 · n20/D 1.574(lit.)
- Flammpunkt
- 230 °F · >230 °F
- storage temp.
- Inert atmosphere,Room Temperature
- Löslichkeit
- sol most organic solvents; reacts with protic solvents such as alcohols, acids, amines, water.
- Aggregatzustand
- clear liquid
- Farbe
- Colorless to Light yellow to Light orange
- Wichte
- 1.128 · 1.128
- Wasserlöslichkeit
- reacts
- BRN
- 2937445 · 2937445
- InChI
- 1S/C13H13ClSi/c1-15(14,12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11H,1H3
- InChIKey
- OJZNZOXALZKPEA-UHFFFAOYSA-N
- SMILES
- C[Si](Cl)(c1ccccc1)c2ccccc2
- CAS Datenbank
- 144 · 144-79-6(CAS DataBase Reference)
- NIST chemische Informationen
- Silane, chloromethyldiphenyl-(144-79-6)
- EPA chemische Informationen
- Silane, chloromethyldiphenyl- (144-79-6)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 44 reports by companies from 3 notifications to the ECHA C&L Inventory.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Gefahrenhinweise
Regulatory Information
Chemical: Silane, chloromethyldiphenyl-
Benzene, 1,1'-(chloromethylsilylene)bis- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzene, 1,1'-(chloromethylsilylene)bis- 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)
Regulatorische Informationen
Regulatory Information
Chemical: Silane, chloromethyldiphenyl-
Benzene, 1,1'-(chloromethylsilylene)bis- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzene, 1,1'-(chloromethylsilylene)bis- 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)
Sicherheitsdaten
- F
- 10-21
- wgk
- 1
- tsca
- TSCA listed
- ridadr
- UN 2987 8/PG 2
- hs_code
- 29319090
- risk_code
- 34-37
- hazard_code
- C
- safety_code
- 26-36/37/39-45-25
- hazard_class
- 8
- packing_group
- II
- Speicherklasse
- 8A - Combustible corrosive hazardous materials
- Hazard Classifications
- Eye Dam. 1Skin Corr. 1B
Chemie und Industrie
Verwendung und Herstellung
General Manufacturing Information
All Other Basic Inorganic Chemical Manufacturing
Benzene, 1,1'-(chloromethylsilylene)bis-: ACTIVE
Anwendungen
VerwendenMethyldiphenylchlorosilane can be used as protecting group for alcohols; reacts with carboxylic acids and sulfoximes; C-silylates lithium ester enolates.
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