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Azidotrimethylsilan

Azidotrimethylsilane Struktur
4648-54-8
CAS-Nr.
4648-54-8
Bezeichnung:
Azidotrimethylsilan
Englisch Name:
Azidotrimethylsilane
Synonyma:
TMSN3;TRIMETHYLSILYL AZIDE;TMSiA;decomposes;(CH3)3SiN3;AzidotrimethyL;Trimethylazidosilane;Three methyl azide silane;CFS-548;Co-Formula CFS-548
CBNumber:
CB3444416
Summenformel:
C3H9N3Si
Molgewicht:
115.21
MOL-Datei:
4648-54-8.mol

Azidotrimethylsilan Eigenschaften

Schmelzpunkt:
-95°C
Siedepunkt:
92-95 °C(lit.)
Dichte
0.876 g/mL at 20 °C(lit.)
Brechungsindex
n20/D 1.415(lit.)
Flammpunkt:
74 °F
storage temp. 
2-8°C
L?slichkeit
Miscible with toluene, dichloromethane, diethyl ether and most organic solvents.
Aggregatzustand
Liquid
Wichte
0.868
Farbe
Clear colorless to slightly yellow
Wasserl?slichkeit
decomposes
Sensitive 
Moisture Sensitive
Hydrolytic Sensitivity
8: reacts rapidly with moisture, water, protic solvents
BRN 
1903730
InChI
1S/C3H9N3Si/c1-7(2,3)6-5-4/h1-3H3
InChIKey
SEDZOYHHAIAQIW-UHFFFAOYSA-N
SMILES
C[Si](C)(C)N=[N+]=[N-]
CAS Datenbank
4648-54-8(CAS DataBase Reference)
NIST chemische Informationen
Azidotrimethylsilane(4648-54-8)
EPA chemische Informationen
Azidotrimethylsilane (4648-54-8)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher F,T,N
R-S?tze: 11-23/24/25-50/53-29
S-S?tze: 16-36/37/39-45-8-57-36/37-29
RIDADR  UN 1992 3/PG 2
WGK Germany  3
10-33
Selbstentzündungstemperatur 300 °C
TSCA  TSCA listed
HazardClass  3
PackingGroup  II
HS Code  29310095
Speicherklasse 3 - Flammable liquids
Hazard Classifications Acute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Flam. Liq. 2
Bildanzeige (GHS) Flame (GHS02)Skull and Crossbones (GHS06)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H225 Flüssigkeit und Dampf leicht entzündbar. Entzündbare Flüssigkeiten Kategorie 2 Achtung P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
Sicherheit
P210 Von Hitze, hei?en Oberfl?chen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Azidotrimethylsilan Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R11:Leichtentzündlich.
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R50/53:Sehr giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche Wirkungen haben.
R29:Entwickelt bei Berührung mit Wasser giftige Gase.

S-S?tze Betriebsanweisung:

S16:Von Zündquellen fernhalten - Nicht rauchen.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S8:Beh?lter trocken halten.
S57:Zur Vermeidung einer Kontamination der Umwelt geeigneten Beh?lter verwenden.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S29:Nicht in die Kanalisation gelangen lassen.

Chemische Eigenschaften

Azidotrimethylsilane (TMSN3) is a clear colorless to slightly yellow liquid. It shows very slow decomposition at high temperatures. It is a very commonly used azide source and has been used in the synthesis of aminotriazole ligands. Azidotrimethylsilane can be easily synthesised by adding chlorotrimethylsilane dropwise to a stirred solution of NaN3 in diethylene glycol dimethyl ether.

Verwenden

Many applications of TMSA in organic synthesis have been reported but only representative examples are described herein.Substitution Reactions. Benzyl,allyl,and substituted alkyl halides are converted to the corresponding azides in 60–100% yields via reactions with TMSA under neutral conditions in a nonaqueous solvent (eq 1).By using tin(IV) chloride as a catalyst, secondary and tertiary cyclic and polycyclic halides are similarly transformed into the corresponding azides in 50–92% yields (eq 1).
Substitution Reactions of Azidotrimethylsilane

synthetische

Azidotrimethylsilane may be synthesised by reacting trimethylchlorosilane with sodium azide in hexamethylphosphoramidic triamide. several methods for the synthesis of this azide have been reported.The procedure involving aluminum chloride is not recommended, since an explosive product is formed.Azidotrimethylsilane is now commercially available, and a representative synthetic procedure is as follows. A mixture of sodium azide and chlorotrimethylsilane is refluxed in di-n-butyl ether for 2 days and the azide is safely distilled directly from the reaction vessel. Purer compound (99% content) is obtained by redistillation of the product. Several improved conditions have been reported for the preparation of this azide.In these procedures, trimethylsilyl chloride is reacted with sodium azide either neat or in a high boiling point solvent, such as a mixture of silicone oil and polyethylene glycol. Distillation of the crude product usually provides trimethylsilyl azide (TMSA) in high purity (97.9%) and yield (97%).

l?uterung methode

Distil the azide through a Vigreux column (p 11) in a N2 atmosphere maintaining the oil bath temperature thermostat at 135-140o . Check the purity by 1H NMR [CHCl3, : single peak at 13cps from Me4Si]. Likely impurities are siloxane hydrolysis products. The azide is thermally stable even at 200o when it decomposes slowly without explosive violence. All the same, it is advisable to carry out the distillation behind a thick safety screen in a fumehood because unforseen EXPLOSIVE azides may be formed on long standing. [Birkofer & Wagner Org Synth Coll Vol VI 1030 1988.]

Azidotrimethylsilan Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Azidotrimethylsilan Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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4648-54-8(Azidotrimethylsilan)Verwandte Suche:


  • azidotrimethyl-silan
  • Silane, azidotrimethyl-
  • Silane,azidotrimethyl-
  • Azidotrimethylsilane ,95%
  • Azidotrimethylsilane,Trimethylsilyl azide
  • TRIMETHYLSILYL AZIDE FOR SYNTHESIS
  • AzidotriMethylsilane, 97% 10ML
  • TriMethylsilyl azid
  • zidotrimethylsilane
  • 1-(Trimethylsilyl)-1,3-diaza-2-azoniapropadiene-3-ide
  • AZIDOTRIMETHYLSILANE
  • Trimethylsilylazide,95%
  • Trimethylsilylazide,typically95%
  • Azidotrimethyl silane(97%)
  • Trimethylsilylazide, typically 95%
  • Trimethylsilyl azide (TMSA)
  • Trimethylsilyl azide,98+%
  • Co-Formula CFS-548
  • CFS-548
  • TrimethylsilylAzide>
  • Trimethylsilyl azide, 93%, for synthesis
  • Azidotrimethylsilane, 94%,
  • TMSiA
  • (CH3)3SiN3
  • Trimethylazidosilane
  • Three methyl azide silane
  • Azide trimethylsilane
  • Trimethyl silicon azide
  • AzidotrimethyL
  • decomposes
  • TMSN3
  • TRIMETHYLSILYL AZIDE
  • 4648-54-8
  • 648-54-8
  • C3H10N2Si
  • C3H9N3Si
  • Azidation/Diazo Transfer
  • Si (Classes of Silicon Compounds)
  • Silicon Compounds (for Synthesis)
  • Si-N Compounds
  • Trimethylsilylazide, etc.
  • Synthetic Reagents
  • C-X Bond Formation (Non-Halogen)
  • Si (Classes of Silicon Compounds)
  • Silicon Compounds (for Synthesis)
  • Si-N Compounds
  • Synthetic Organic Chemistry
  • Trimethylsilylazide, etc.
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