Detail of "3908-55-2"

CAS Number:
3908-55-2
Name:
Silane,trimethyl(methylthio)-
Molecular Structure:
Formula:
C₄H₁₂SSi
Molecular Weight:
120.2886
Synonyms:
(Methylthio)trimethylsilane;Methyl trimethylsilyl sulfide;Trimethyl(methylthio)silane;
EINECS:
223-466-9
Density:
0.833g/cm³
Boiling Point:
112 °C at 760 mmHg
Flash Point:
3.3 °C
Hazard Symbols:
Xi
Risk Codes:
10-36/37/38
Safety:
26-36 Details
Transport Information:
UN 1993

Display：

(METHYLTHIO)TRIMETHYLSILANE

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Fluorocarbon derivatives of nitrogen: Fluorocarbon derivatives of nitrogen. Part IX. Synthesis of some new 3,3,4,4,5,5-hexafluoro-2,6-bis(trifluoromethyl)-1-azacyclohexenes. Abed-Rabboh, Mohammad; Banks, Ronald E.; Nickkho-Amiry, Mahmood; Oppenheim, Charles (Inst. Sci. Technol., Univ. Manchester, Manchester M60 1QD, UK). J. Fluorine Chem.Several substances with their cas registry numbers 3908-55-2 and 4648-54-8 may be metioned in this study., 23(3), 283-92 (English) 1983. CODEN: JFLCAR. ISSN: 0022-1139. DOCUMENT TYPE: Journal CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) Treating perfluoro-(2,6-dimethyl-1-azacyclohexene) with Et3SiH, ClSiMe3, MeSSiMe3, and Me3SiN3 gave azacyclohexenes I (R = H, Cl, MeS, N3). I (R = MeS) was converted into its 6H-analog by toluene-4-thiol; treating perfluoro-(2,6-dimethyl-1-azacyclohexene) with AlCl3 and NaN3, resp., gave alternative routes to I (R = Cl, N3). .

Amino-substituted cyclohepta[c]pyrrolium salts and 6-amino-2-azaazulene from cyclohepta[c]pyrrol-6(2H)-one: Amino-substituted cyclohepta[c]pyrrolium salts and 6-amino-2-azaazulene from cyclohepta[c]pyrrol-6(2H)-one. Seitz, Gunther; The, Han Sui (Pharm. Chem. Inst., Philipps-Univ. Marburg, Marburg/Lahn D-3550, Fed. Rep. Ger.). Synthesis, (2), 119-21 (German) 1984. CODEN: SYNTBF.Several substances with their cas registry numbers 15097-49-1 and 3908-55-2 may be metioned in this study. ISSN: 0039-7881. DOCUMENT TYPE: Journal CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) 1,3-Dimethylcyclohepta[c]pyrrol-6(2H)-one was chlorinated with (COCl)2 and treated with LiClO4 to give I.HClO4 (R = Cl) (II). This was treated with Me3SiNR21 [R1 = Me; R21 = (CH2)5, (CH2)6, O(CH2CH2)2] to give I.HClO4 (R = NR21), which gave the free bases on treatment with Me3COK. II reacted with Me3SiSMe to give I (R = MeS). .